Peptidomimetic macrocycles and uses thereof

ABSTRACT

Methods for treating solid tumor, determined to lack a p53 deactivation mutation, in a subject are provided. Also provided are peptidomimetic macrocycles for use in treatment of a solid tumor, determined to lack a p53 deactivation mutation, in a subject.

CROSS REFERENCE

This application calims priority to U.S. Provisional Application No. 62/054,861, filed Sep. 24, 2014, U.S. Provisional Application No. 62/213,831, filed Sep. 3, 2015 and U.S. Provisional Application No. 62/216,670, filed Sep. 10, 2015 each of which is incorporated herein by reference in its entirety.

BACKGROUND OF THE INVENTION

The human transcription factor protein p53 induces cell cycle arrest and apoptosis in response to DNA damage and cellular stress, and thereby plays a critical role in protecting cells from malignant transformation. The E3 ubiquitin ligase MDM2 (also known as HDM2 or human double minute 2) negatively regulates p53 function through a direct binding interaction that neutralizes the p53 transactivation activity, leads to export from the nucleus of p53 protein, and targets p53 for degradation via the ubiquitylation-proteasomal pathway. Loss of p53 activity, either by deletion, mutation, or MDM2 overexpression, is the most common defect in human cancers. Tumors that express wild type p53 are vulnerable to pharmacologic agents that stabilize or increase the concentration of active p53. In this context, inhibition of the activities of MDM2 has emerged as a validated approach to restore p53 activity and resensitize cancer cells to apoptosis in vitro and in vivo. MDMX (also known as MDM4, HDM4 or human double minute 4) has more recently been identified as a similar negative regulator of p53, and studies have revealed significant structural homology between the p53 binding interfaces of MDM2 and MDMX.MDMX has also been observed to be overexpressed in human tumors. The p53-MDM2 and p53-MDMX protein-protein interactions are mediated by the same 15-residue alpha-helical transactivation domain of p53, which inserts into hydrophobic clefts on the surface of MDM2 and MDMX. Three residues within this domain of WT p53 (F19, W23, and L26) are essential for binding to MDM2 and MDMX.

There remains a considerable need for methods for treating solid tumor. Provided herein are compounds capable of binding to and modulating the activity of p53, MDM2 and/or MDMX. Also provided herein are pharmaceutical formulations comprising p53-based peptidomimetic macrocycles that modulate an activity of p53. Also provided herein are pharmaceutical formulations comprising p53-based peptidomimetic macrocycles that inhibit the interactions between p53, MDM2 and/or MDMX proteins. Further, provided herein are methods for treating diseases including but not limited to solid tumors and other hyperproliferative diseases.

SUMMARY OF THE INVENTION

In one aspect, the disclosure provides a method of treating solid tumor determined to lack a p53 deactivating mutation, in a human subject, wherein the method comprises administering to the human subject a therapeutically effective amount of a peptidomimetic macrocycle or a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins. In some embodiments, the peptidomimetic macrocycle disrupts the interaction between p53 and MDM2 and MDMX.

In another aspect, the disclosure provides a method of treating a solid tumor that lacks a p53 deactivating mutation, in a human subject in need thereof wherein the method comprises administering to the human subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins.

In another aspect, the disclosure provides a method of treating a solid tumor that has a p53 deactivating mutation in a p53 gene, in a human subject in need thereof wherein the method comprises administering to the human subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins.

In another aspect, the disclosure provides a method of treating a solid tumor in a human subject in need thereof, wherein the method comprises administering to the human subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins and wherein the solid tumor is not negative for p53 protein expression (such as solid tumors that express wild-type p53 protein or mutated p53 protein with partial functionality).

In another aspect, the disclosure provides a method of treating a solid tumor in a human subject in need thereof, wherein the method comprises administering to the human subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins and wherein the solid tumor expresses a p53 protein with a gain of function mutation (such as a super apoptotic p53).

In another aspect, the disclosure provides a method of treating a solid tumor in a human subject in need thereof, wherein the method comprises administering to the human subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins and wherein the solid tumor express a p53 protein with a mutation that causes a partial loss of function.

In another aspect, the disclosure provides a method of treating a solid tumor a human subject in need thereof wherein the method comprises administering to the human subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins and wherein cells in the solid tumor express p53 from only a single genomic copy of the p53 gene (for example where the cells have a copy loss mutation, e.g., are haploinsufficient).

In another aspect, the disclosure provides a method of treating a solid tumor a human subject in need thereof wherein the method comprises administering to the human subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins and wherein the solid tumor express a p53 protein with one or more silent mutations.

In another aspect, the disclosure provides a method of treating a solid tumor a human subject in need thereof wherein the method comprises administering to the human subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins and wherein cells in the solid tumor are negative for p53 expression.

In another aspect, the disclosure provides a method of treating a solid tumor that has a p53 deactivating mutation in a p53 gene, in a human subject in need thereof wherein the method comprises administering to the human subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins and wherein cells in the solid tumor have the p53 deactivating mutation in one copy of the p53 gene. In some embodiments, the cells in the solid tumor have a second p53 deactivating mutation in a second copy of a p53 gene. In some embodiments, the p53 deactivating mutation in one copy of the p53 gene is the same as the second p53 deactivating mutation in the second copy of a p53 gene. In some embodiments, the p53 deactivating mutation in one copy of the p53 gene is different from the second p53 deactivating mutation in the second copy of a p53 gene.

In some embodiments, the p53 deactivating mutation in the p53 gene results in the lack of p53 protein expression from the p53 gene or in expression of partial a p53 protein with partial loss of function. In some embodiments, the second p53 deactivating mutation in the second copy of a p53 gene results in the lack of p53 protein expression from the p53 gene or in expression of partial a p53 protein with partial loss of function.

In some embodiments of the methods described herein, the cells of the solid tumor have at least one mutation in a copy of a p53 gene, wherein the mutation eliminates or reduces the or activity of a p53 protein expressed from the copy of the p53 gene, as compared to wild type p53 expressed from a copy of a non-mutated p53 gene.

In another aspect, the disclosure provides a method of treating a solid tumor in a human subject in need thereof wherein the method comprises administering to the human subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins.

In some embodiments, the peptidomimetic macrocycle used in the various methods described herein is a peptidomimetic macrocycle that disrupts the interaction between p53 and MDM2 and MDMX.

In some embodiments, the various methods described herein further comprise determining the lack of the p53 deactivating mutation in the solid tumor prior to the administration of the pharmaceutical composition. In some embodiments, the determining the lack of the p53 deactivating mutation comprises confirming the presence of wild type p53 in the solid tumor.

In some embodiments, the various methods described herein further comprise determining a presence of a p53 gain of function mutation in the solid tumor.

In some embodiments, the various methods described herein further comprise determining a presence of a deactivating mutation of p53 in the solid tumor.

In some embodiments, the various methods described herein further comprise determining a presence of a copy loss mutation of p53 in the solid tumor.

In some embodiments, the various methods described herein further comprise determining a presence of a partial loss of function mutation of P53 in the solid tumor.

In some embodiments, the methods described herein can further comprise confirming the lack of the p53 deactivating mutation in the solid tumor, prior to the administration of the peptidomimetic macrocycle. For example, confirming the presence of wild type p53 in the solid tumor.

In some embodiments, the methods described herein can further comprise confirming a presence of a p53 gain of function mutation in the solid tumor.

In some embodiments, the methods described herein can further comprise confirming a presence of a deactivating mutation of p53 in the solid tumor.

In some embodiments, the methods described herein can further comprise confirming a presence of a copy loss mutation of p53 in the solid tumor.

In some embodiments, the methods described herein can further comprise confirming a presence of a partial loss of function mutation of P53 in the solid tumor.

In various embodiments, the determining or confirming is performed within 3 years, 2 years, within 1 year, within 1-12 months, within 1-3 months, within 1 month, or within 21 days prior to the administration of the peptidomimetic macrocycle.

In various embodiments, the treatment methods provided herein can result in re-activation of the p53 pathway, decreased tumor cell proliferation, increased p53 protein, increased p21, and/or increased apoptosis in the human subject.

The peptidomimetic macrocycle can be administered two or three times a week, for example two times a week. In some examples, the peptidomimetic macrocycle is administered once every 2 or 3 weeks. In other examples the peptidomimetic macrocycle is administered once every 1 or 2 weeks. In some embodiments, the peptidomimetic macrocycle is administered on days 1, 8 and 15 of a 28-day cycle. In other examples the peptidomimetic macrocycle is administered once every week. In some examples, a dose of the pharmaceutical composition is administered on days 1, 4, 8 and 11 of a 21-day cycle.

The amount of the peptidomimetic macrocycle administered is about 0.5-20 mg per kilogram body weight of the human subject, for example 0.5-10 mg per kilogram body weight of the human subject. In some embodiments, the amount of the peptidomimetic macrocycle administered is about 0.04 mg, 0.08 mg, 0.16 mg, 0.32 mg, 0.64 mg, 1.28 mg, 3.56 mg, 7.12 mg, or 14.24 mg per kilogram body weight of the human subject. In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg 10.0 mg, or 20.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered two times a week. In other examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg or 10.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered two times a week. In other examples, 0.32 mg, 0.64 mg, 1.25 mg 2.5 or 5.0 mg per kilogram body weight of the human subject and the pharmaceutical composition is administered two times a week. In some examples, about 0.32 mg, 0.64 mg, 1.25 mg 2.5 or 5.0 mg per kilogram body weight of the human subject and the pharmaceutical composition is administered on day 1, 4, 8, 11 of a 21-day cycle. In some examples, about 0.16 mg, 0.32 mg, 0.64 mg, 1.25 mg, 2.5, 5.0 mg or 10 mg per kilogram body weight of the human subject and the pharmaceutical composition is administered on day 1, 8, and 15 of a 28 day cycle.

In other examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg, 10.0 mg, or 20.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered once a week. In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg or 10.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered once a week.

In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg 10.0 mg, or 20.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered once daily, three, five or seven times in a seven day period. For example, the peptidomimetic macrocycle is administered once daily intravenously, seven times in a seven day period.

In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg, or 10.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered once daily three, five or seven times in a seven day period. For example, the peptidomimetic macrocycle is administered once daily intravenously, seven times in a seven day period.

The peptidomimetic macrocycle can be administered gradually over a period of 0.25-12 h, for example over a period of 0.25 h, 0.5 h, 1 h, 2 h, 3 h, 4 h, 5 h, 6 h, 7 h, 8 h, 9 h, 10 h, 11 h, or 12 h. In some examples, the peptidomimetic macrocycle is administered over a period of 0.25-2.0 h. In some embodiments, the peptidomimetic macrocycle is gradually administered over a period of 1 h. In other embodiments, the peptidomimetic macrocycle is gradually administered over a period of 2 h.

The method provided herein can result in reduction of tumor volume. For example, treatment according to methods provided herein can result in about 95%, 90%, 85%, 80%, 75%, 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30%, 25%, 20%, 15%, 10%, or 5% reduction in tumor volume within a period of 1 month after treatment initiation. In some example, the treatment results in at least 60%, 65%, 70%, 75%, 80%, 85%, 90%, or 95% reduction in tumor volume within a period of 1 month after treatment initiation. In some examples, the treatment results in about 95%, 90%, 85%, 80%, 75%, 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30%, 25%, 20%, 15%, 10%, or 5% reduction in tumor volume within a period of 1 year after treatment initiation. In some embodiments, the treatment results in at least 60%, 65%, 70%, 75%, 80%, 85%, 90%, or 95% reduction in tumor volume within a period of 1 year after treatment initiation. In some examples, the treatment results in about 95%, 90%, 85%, 80%, 75%, 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30%, 25%, 20%, 15%, 10%, or 5% reduction in tumor volume within a period of 6 months after treatment initiation. In some examples, the treatment results in at least 60%, 65%, 70%, 75%, 80%, 85%, 90%, or 95% reduction in tumor volume within a period of 6 months after treatment initiation. In some examples, the treatment results in about 95%, 90%, 85%, 80%, 75%, 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30%, 25%, 20%, 15%, 10%, or 5% reduction in tumor volume within a period of 3 months after treatment initiation. In some examples, the treatment results in at least 60%, 65%, 70%, 75%, 80%, 85%, 90%, or 95% reduction in tumor volume within a period of 3 months after treatment initiation. In some embodiments, the solid tumor is a stable disease. In some embodiments, the solid tumor is a progressive disease.

In some embodiments, the methods provided herein can result in an increased survival time of the human subject as compared to the expected survival time of the human subject if the human subject was not treated with the peptidomimetic macrocycle. In some examples, the increase in the survival time of the human subject is at least 30 days, at least 3 months, at least 6 months or at least 1 year.

The in vivo circulating half-life of the peptidomimetic macrocycle is about 1 h-12 h, for example about 1 h, 2 h, 3 h, 4 h, 5 h, 6 h, 7 h, 8 h, 9 h, 10 h or 12 h. In some examples, the in vivo circulating half-life of the peptidomimetic macrocycle is about 4 h, about 6 h.

The biological tissue half-life of the peptidomimetic macrocycle is about 1 h-12 h, for example about 1 h, 2 h, 3 h, 4 h, 5 h, 6 h, 7 h, 8 h, 9 h, 10 h or 12 h. In some examples, the biological tissue half-life of the peptidomimetic macrocycle is about 10 h.

In some embodiments, the human subject treated in accordance to the methods of the disclosure is refractory and/or intolerant to one or more other treatment of the solid tumor. In some embodiments, the human subject has had at least one unsuccessful prior treatment and/or therapy of the solid tumor.

In some embodiments, the solid tumor expresses wild-type p53 protein.

The solid tumor treated by the methods of the disclosure is selected from a group consisting of pancreatic cancer, bladder cancer, colon cancer, liver cancer, colorectal cancer, breast cancer, prostate cancer, renal cancer, hepatocellular cancer, lung cancer, ovarian cancer, cervical cancer, gastric cancer, esophageal cancer, head and neck cancer, melanoma, neuroendocrine cancers, CNS cancers, brain tumors, bone cancer, skin cancer, ocular tumor, rectal cancer, choriocarcinoma (tumor of the placenta), sarcoma and soft tissue cancer, testicular cancer, gall bladder cancer, and biliary cancer. In some embodiments, the solid tumor is selected from a group consisting of bladder cancer, bone cancer, breast cancer, cervical cancer, CNS cancer, colon cancer, ocular tumor, renal cancer, liver cancer, lung cancer, pancreatic cancer, choriocarcinoma (tumor of the placenta), prostate cancer, sarcoma, skin cancer, soft tissue cancer, gastric cancer, gall bladder cancer, biliary cancer, renal cancer, or neuroendocrine cancer. The ocular tumor can be choroidal nevus, choroidal melanoma, choroidal metastasis, choroidal hemangioma, choroidal osteoma, iris melanoma, uveal melanoma, melanocytoma, metastasis retinal capillary hemangiomas, congenital hypertrophy of the RPE, RPE adenoma or retinoblastoma. In some embodiments, the solid tumor is selected from non-small cell lung cancer, small-cell lung cancer, colon cancer, CNS cancer, melanoma, ovarian cancer, renal cancer, prostate cancer and breast cancer. In some embodiments, the solid tumor is breast cancer. In some embodiments, the solid tumor is gall bladder cancer. In some embodiments, the solid tumor is the solid tumor is biliary cancer. In some embodiments, the solid tumor is neuroendocrine cancer. In some embodiments, the solid tumor is bone cancer. In some embodiments, the solid tumor is osteosarcoma. In some embodiments, the solid tumor is skin cancer. In some embodiments, the solid tumor is melanoma.

In some examples, the solid tumor treated by the methods of the disclosure is not a HPV positive cancer.

In some examples, the solid tumor treated by the methods of the disclosure is not HPV positive cervical cancer, HPV positive anal cancer or HPV positive head and neck cancer, such as oropharyngeal cancers.

In some embodiments, the peptidomimetic macrocycle is administered intravenously.

In some embodiments, the methods of the disclosure further comprise administering in addition to the peptidomimetic macrocycle or pharmaceutically acceptable salt thereof, a therapeutically effective amount of at least one additional therapeutic agent and/or therapeutic procedure to the human subject.

In some embodiments, the human subject exhibits a complete response to the treatment. In some embodiments, the human subject exhibits a partial response to the treatment.

In some embodiments, the methods of the disclosure further comprise determining clinical activity of the administered peptidomimetic macrocycle. The clinical activity can be determined by an imaging method selected from a group consisting of computed tomography (CT), magnetic resonance imaging (MRI), and bone scanning.

The methods of the disclosure can further comprise obtaining a biological sample from the human subject at one or more specific time-points and analyzing the biological sample with an analytical procedure. The biological samples can be used for biomarker assessment, pharmacokinetic assessment, immunogenicity assays and/or pharmacodynamic assessment. The pharmacokinetic assessment can comprise studying the level of the peptidomimetic macrocycle and/or its metabolites in the biological sample at the specific time-points. The pharmacodynamic assessment can comprise studying the level of p53, MDM2, MDMX, p21 and/or caspase in the biological sample at the specific time-points.

The analytical procedure can be selected from a group comprising blood chemistry analysis, chromosomal translocation analysis, needle biopsy, tissue biopsy, fluorescence in situ hybridization, laboratory biomarker analysis, immunohistochemistry staining method, flow cytometry, or a combination thereof. The methods can further comprise tabulating and/or plotting results of the analytical procedure. The one or more specific time-points can comprise a time-point before the administration of the peptidomimetic macrocycle to the human subject. The one or more specific time-points can comprise a time-point after the administration of the peptidomimetic macrocycle to the human subject. The one or more specific time-points can comprise a time-point before and a time-point after the administration of the peptidomimetic macrocycle to the human subject. The one or more specific time-points comprise multiple time-points before and after the administration of the peptidomimetic macrocycle to the human subject. The method can further comprise comparing the biological samples collected before and after the administration of the peptidomimetic macrocycle to the human subject or comparing the biological samples collected at the multiple time-points. The biological sample can be a blood sample or a tumor specimen.

The method of the disclosure can further comprise selecting and/or identifying at least one target lesion in the human subject prior to the administration of the peptidomimetic macrocycle to the human subject. The methods can also comprise measuring cumulative diameters at one or more specific time-points, wherein the cumulative diameter is a sum of the diameters of the at least one target lesions at the specific time-point. The one or more specific time-points, can comprise a time-point after the treatment. The methods can also comprise measuring a baseline sum diameter, wherein the baseline sum diameter is a sum of the diameters of the at least one target lesions prior to the administration of the pharmaceutical composition to the human subject. In some examples, the treatment in accordance to the methods of the disclosure results in disappearance of the least one target lesion. In some embodiments, after the treatment all pathological lymph nodes in the human subject exhibit a reduction in short axis to less than 10 mm. In some examples, the cumulative diameter at the time-point after the treatment is at least 30% less than the baseline sum diameter. In some examples, the treatment results in neither a sufficient increase nor a sufficient decrease in the cumulative diameters at the one or more specific time-points, taking as reference the baseline sum diameter.

In some examples, the peptidomimetic macrocycle is not an inhibitor of cytochrome P450 isoforms. In some examples, the treatment results in essentially no dose-limiting thrombocytopenia. In some examples, the treatment causes essentially no adverse effects in a normal-hematopoietic organ and/or tissue. In some examples, the treatment results in essentially no adverse event in the human subject that can be possibly, probably, or definitely related to the administration of the peptidomimetic macrocycle. In some examples, the treatment results in essentially no serious adverse event in the human subject that can be probably, probably, or definitely related to the administration of the peptidomimetic macrocycle.

The lack of p53 deactivation mutation can be determined by any known method known in the art. In some examples, the lack of p53 deactivation mutation can be determined by DNA sequencing of the nucleic acid encoding the p53 protein. In some examples, the lack of p53 deactivation mutation can be determined by RNA array based testing. In some examples, the lack of p53 deactivation mutation can be determined by RNA analysis. In some examples, the lack of p53 deactivation mutation can be determined by polymerase chain reaction (PCR).

In some embodiments, the p53 deactivating mutation can comprise mutations in DNA-binding domain of the protein. In some embodiments, the p53 deactivating mutation can comprise missense mutation. In some embodiments, the p53 deactivating mutation is a dominant deactivating mutation. In some embodiments, the p53 deactivating mutation comprises one or more mutations selected from a groups consisting of V173L, R175H, G245C, R248W, R249S and R273H. In some embodiments, the p53 deactivating mutation comprises one or more of mutations shown in Table 1a. In some embodiments, the p53 gain of function mutation comprises one or more of mutations shown in Table 1b.

In another aspect, the disclosure provides a method of treating solid tumor in a human subject determined to lack a p53 deactivating mutation, wherein the method comprises administering to the human subject 0.5-20 mg, for example 0.5-10 mg of a peptidomimetic macrocycle per kilogram body weight of the human subject or a pharmaceutically acceptable salt thereof on days 1, 8 and 15 of a 28-day cycle. In some embodiments, the amount of the peptidomimetic macrocycle entered on day 8 and/or day 15 is greater than the amount of the peptidomimetic macrocycle entered on day 1. In some embodiments, the peptidomimetic macrocycle entered on day 8 and/or day 15 is equal than the amount of the peptidomimetic macrocycle entered on day 1. In some embodiments, t the peptidomimetic macrocycle entered on day 1 and/or day 8 is greater than the amount of the peptidomimetic macrocycle entered on day 15. In some embodiments, an equal amount of the peptidomimetic macrocycle is administered on days 1, 8 and 15. In some embodiments, the 28-day cycle is repeated 2 or 3 times.

In another aspect, the disclosure provides a method of treating solid tumor in a human subject, wherein the method comprises administering to the human subject 0.32-10 mg of a peptidomimetic macrocycle per kilogram body weight of the human subject or a pharmaceutically acceptable salt thereof on days 1, 4, 8 and 11 of a 21-day cycle. In some embodiments, the solid tumor is determined to lack a p53 deactivating mutation. In some embodiments, 0.32 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject or the pharmaceutically acceptable salt thereof is administered on days 1, 4, 8 and 11 respectively of a 21-day cycle. In some embodiments, 0.64 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject or the pharmaceutically acceptable salt thereof is administered on days 1, 4, 8 and 11 respectively of a 21-day cycle. In some embodiments, 1.25 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject or the pharmaceutically acceptable salt thereof is administered on days 1, 4, 8 and 11 respectively of a 21-day cycle. In some embodiments, 2.5 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject or the pharmaceutically acceptable salt thereof is administered on days 1, 4, 8 and 11 respectively of a 21-day cycle. In some embodiments, 5.0 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject or the pharmaceutically acceptable salt thereof is administered on days 1, 4, 8 and 11 respectively of a 21-day cycle.

In various embodiments, the peptidomimetic macrocycle used in the methods described herein comprises an amino acid sequence which is at least about 60%, 70%, 80%, 90%, or 95% identical to an amino acid sequence in any of Table 3, Table 3a, Table 3b, and Table 3c, wherein the peptidomimetic macrocycle has the formula:

wherein: each A, C, D and E is independently an amino acid; each B is independently an amino acid,

[—NH-L₃-CO—], [—NH-L₃-SO₂—], or [—NH-L₃-]; each R₁ and R₂ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids; each R₃ independently is hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅; each L and L′ is independently a macrocycle-forming linker of the formula -L₁-L₂-; each L₁, L₂, and L₃ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄—K—R₄—]_(n), each being optionally substituted with R₅; each R₄ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene; each K is independently O, S, SO, SO₂, CO, CO₂, or CONR₃; each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₇ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue; each R₈ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue; each v is independently an integer; each w is independently an integer from 3-1000; u is an integer from 1-10; each x, y and z is independently an integer from 0-10; and each n is independently an integer from 1-5.

In various embodiments, the peptidomimetic macrocycle used in the methods described herein has formula:

wherein: each of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ is individually an amino acid, wherein at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8) or Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9), where each X₄ and X₁₁ is independently an amino acid; each D and E is independently an amino acid; each R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids; each L or L′ is independently a macrocycle-forming linker each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₇ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue; each R₈ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue; v is an integer from 1-1000; w is an integer from 0-1000.

In some embodiments, at least one of the macrocycle-forming linker in the Formulas described herein has a formula -L₁-L₂-, wherein

each L₁ and L₂ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄—K—R₄—]_(n), each being optionally substituted with R₅; each R₄ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene; each K is independently O, S, SO, SO₂, CO, CO₂, or CONR₃; each R₃ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅; and each n is independently an integer from 1-5.

In some embodiments, at least one of the macrocycle-forming linker in the Formulas described herein each w is independently an integer from 3-1000, for example 3-500, 3-200, 3-100, 3-50, 3-30, 3-20, or 3-10.

In some embodiments, Xaa5 is Glu or an amino acid analog thereof.

In some embodiments, each E is independently Ala (alanine), Ser (serine) or an analog thereof.

In some embodiments, [D]v is -Leu₁-Thr₂.

In some embodiments, w is 3-10. In some embodiments, w is 3-6. In some embodiments, w is 6-10. In some embodiments, w is 6.

In some embodiments, v is 1-10. In some embodiments, v is 2-10. In some embodiments, v is 2-5. In some embodiments, v is 2.

In some embodiments, each L₁, L₂ and L₃ in the Formulas described herein are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, or heterocycloarylene, each being optionally substituted with R₅.

In some embodiments, each L₁, L₂ and L₃ are independently alkylene or alkenylene.

In some embodiments, L is alkylene, alkenylene, or alkynylene. In some embodiments, L is alkylene. In some embodiments, L is C3-C16 alkylene. In some embodiments, L is C10-C14 alkylene.

In some embodiments, each R₁ and R₂ in the Formulas described herein are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-. In some embodiments, R₁ and R₂ are H. In some embodiments, each R₁ and R₂ are independently alkyl. In some embodiments, R₁ and R₂ are methyl.

In some embodiments, x+y+z in the Formulas described herein is 6.

In some embodiments, u in the Formulas described herein is 1.

The some embodiments, peptidomimetic macrocycles comprise at least one amino acid which is an amino acid analog. In some embodiments, the peptidomimetic macrocycle is chosen from the peptidomimetic macrocycles shown in Table 3c.

In one aspect, the disclosure provides a method of identifying one or more solid tumor biomarkers in a human subject lacking a p53 deactivating mutation, comprising administering to the human subject a therapeutically effective amount of a peptidomimetic macrocycle described herein. In some examples, the biomarkers are selected from a group comprising p53 status, MDM2 expression level and MDMX expression level.

In the various embodiments, the pharmaceutical composition comprises the pharmaceutically acceptable salt of the peptidomimetic macrocycle. In some embodiments, the pharmaceutically acceptable salt is a sodium salt, potassium salt or calcium salt. In some embodiments, the pharmaceutically acceptable salt is a sodium salt.

INCORPORATION BY REFERENCE

All publications, patents, and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication, patent, or patent application was specifically and individually indicated to be incorporated by reference.

BRIEF DESCRIPTION OF THE DRAWINGS

The novel features of the invention are set forth with particularity in the appended claims. A better understanding of the features and advantages of the present invention will be obtained by reference to the following detailed description that sets forth illustrative embodiments, in which the principles of the invention are utilized, and the accompanying drawings of which:

FIG. 1. Shows human wild type P53 protein sequence.

FIG. 2. Shows an exemplary dose level and Dose Regimen.

FIG. 3. Shows an exemplary dosing overview.

FIG. 4. Shows the amount of Aileron peptide-1 administered for each dose level (DL) and dose regimen.

FIG. 5. Shows an exemplary dose escalation strategy of the disclosure.

FIG. 6. Shows one way Aileron peptide-1 was designed to inhibit both MDMX and MDM2, to reactivate WT p53.

FIG. 7. Shows potential indications of Aileron peptide-1 (from orphan indications or large market opportunities).

FIG. 8. Shows the effect of Aileron peptide-1 across a variety of different cancers.

FIG. 9. Shows the effect of Aileron peptide-1 administered by an intravenous, or IV, injection in an MDMX-driven MCF-7 breast cancer xenograft model

FIG. 10. Shows dose escalation based on a “3+3” dose escalation design.

FIGS. 11a and 11b Show drug concentration (measured or projected) in dose levels for Cohorts.

FIG. 12. Shows the pharmacokinetic model of Aileron peptide-1 which shows a 2-compartment, parallel nonlinear Michaelis-Menten clearance and linear elimination.

FIG. 13. Shows dose dependent increase of MIC-1.

FIG. 14. Shows that patients who have completed at least two cycles of treatment have stable disease. Aileron peptide-1 shows a stable disease rate.

FIG. 15. Shows that Aileron peptide 1 shows on target activation of p21 and p53 in patient blood cells.

DETAILED DESCRIPTION OF THE INVENTION

While preferred embodiments of the present disclosure have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will now occur to those skilled in the art without departing from the disclosure. It should be understood that various alternatives to the embodiments of the disclosure described herein can be employed in practicing the disclosure. It is intended that the following claims define the scope of the disclosure and that methods and structures within the scope of these claims and their equivalents be covered thereby.

DEFINITIONS

As used herein, the term “macrocycle” refers to a molecule having a chemical structure including a ring or cycle formed by at least 9 covalently bonded atoms.

As used herein, the term “peptidomimetic macrocycle” or “crosslinked polypeptide” refers to a compound comprising a plurality of amino acid residues joined by a plurality of peptide bonds and at least one macrocycle-forming linker which forms a macrocycle between a first naturally-occurring or non-naturally-occurring amino acid residue (or analog) and a second naturally-occurring or non-naturally-occurring amino acid residue (or analog) within the same molecule. Peptidomimetic macrocycle include embodiments where the macrocycle-forming linker connects the a carbon of the first amino acid residue (or analog) to the α carbon of the second amino acid residue (or analog). The peptidomimetic macrocycles optionally include one or more non-peptide bonds between one or more amino acid residues and/or amino acid analog residues, and optionally include one or more non-naturally-occurring amino acid residues or amino acid analog residues in addition to any which form the macrocycle. A “corresponding uncrosslinked polypeptide” when referred to in the context of a peptidomimetic macrocycle is understood to relate to a polypeptide of the same length as the macrocycle and comprising the equivalent natural amino acids of the wild-type sequence corresponding to the macrocycle.

As used herein, the term “helical stability” refers to the maintenance of a helical structure by a peptidomimetic macrocycle as measured by circular dichroism or NMR. For example, in some embodiments, a peptidomimetic macrocycle exhibits at least a 1.25, 1.5, 1.75 or 2-fold increase in α-helicity as determined by circular dichroism compared to a corresponding uncrosslinked macrocycle.

The term “amino acid” refers to a molecule containing both an amino group and a carboxyl group. Suitable amino acids include, without limitation, both the D- and L-isomers of the naturally-occurring amino acids, as well as non-naturally occurring amino acids prepared by organic synthesis or other metabolic routes. The term amino acid, as used herein, includes, without limitation, α-amino acids, natural amino acids, non-natural amino acids, and amino acid analogs.

The term “α-amino acid” refers to a molecule containing both an amino group and a carboxyl group bound to a carbon which is designated the α-carbon.

The term “β-amino acid” refers to a molecule containing both an amino group and a carboxyl group in a β configuration.

The term “naturally occurring amino acid” refers to any one of the twenty amino acids commonly found in peptides synthesized in nature, and known by the one letter abbreviations A, R, N, C, D, Q, E, G, H, I, L, K, M, F, P, S, T, W, Y and V.

The following table shows a summary of the properties of natural amino acids:

3- 1- Side-chain Letter Letter Side-chain charge Hydropathy Amino Acid Code Code Polarity (pH 7.4) Index Alanine Ala A nonpolar neutral 1.8 Arginine Arg R polar positive −4.5 Asparagine Asn N polar neutral −3.5 Aspartic acid Asp D polar negative −3.5 Cysteine Cys C polar neutral 2.5 Glutamic acid Glu E polar negative −3.5 Glutamine Gln Q polar neutral −3.5 Glycine Gly G nonpolar neutral −0.4 Histidine His H polar positive (10%) −3.2 neutral (90%) Isoleucine Ile I nonpolar neutral 4.5 Leucine Leu L nonpolar neutral 3.8 Lysine Lys K polar positive −3.9 Methionine Met M nonpolar neutral 1.9 Phenylalanine Phe F nonpolar neutral 2.8 Proline Pro P nonpolar neutral −1.6 Serine Ser S polar neutral −0.8 Threonine Thr T polar neutral −0.7 Tryptophan Trp W nonpolar neutral −0.9 Tyrosine Tyr Y polar neutral −1.3 Valine Val V nonpolar neutral 4.2

“Hydrophobic amino acids” include small hydrophobic amino acids and large hydrophobic amino acids. “Small hydrophobic amino acid” are glycine, alanine, proline, and analogs thereof. “Large hydrophobic amino acids” are valine, leucine, isoleucine, phenylalanine, methionine, tryptophan, and analogs thereof. “Polar amino acids” are serine, threonine, asparagine, glutamine, cysteine, tyrosine, and analogs thereof. “Charged amino acids” are lysine, arginine, histidine, aspartate, glutamate, and analogs thereof.

The term “amino acid analog” refers to a molecule which is structurally similar to an amino acid and which can be substituted for an amino acid in the formation of a peptidomimetic macrocycle Amino acid analogs include, without limitation, β-amino acids and amino acids where the amino or carboxy group is substituted by a similarly reactive group (e.g., substitution of the primary amine with a secondary or tertiary amine, or substitution of the carboxy group with an ester).

The term “non-natural amino acid” refers to an amino acid which is not one of the twenty amino acids commonly found in peptides synthesized in nature, and known by the one letter abbreviations A, R, N, C, D, Q, E, G, H, I, L, K, M, F, P, S, T, W, Y and V. Non-natural amino acids or amino acid analogs include, without limitation, structures according to the following:

Amino acid analogs include β-amino acid analogs. Examples of β-amino acid analogs include, but are not limited to, the following: cyclic β-amino acid analogs; β-alanine; (R)-β-phenylalanine; (R)-1,2,3,4-tetrahydro-isoquinoline-3-acetic acid; (R)-3-amino-4-(1-naphthyl)-butyric acid; (R)-3-amino-4-(2,4-dichlorophenyl)butyric acid; (R)-3-amino-4-(2-chlorophenyl)-butyric acid; (R)-3-amino-4-(2-cyanophenyl)-butyric acid; (R)-3-amino-4-(2-fluorophenyl)-butyric acid; (R)-3-amino-4-(2-furyl)-butyric acid; (R)-3-amino-4-(2-methylphenyl)-butyric acid; (R)-3-amino-4-(2-naphthyl)-butyric acid; (R)-3-amino-4-(2-thienyl)-butyric acid; (R)-3-amino-4-(2-trifluoromethylphenyl)-butyric acid; (R)-3-amino-4-(3,4-dichlorophenyl)butyric acid; (R)-3-amino-4-(3,4-difluorophenyl)butyric acid; (R)-3-amino-4-(3-benzothienyl)-butyric acid; (R)-3-amino-4-(3-chlorophenyl)-butyric acid; (R)-3-amino-4-(3-cyanophenyl)-butyric acid; (R)-3-amino-4-(3-fluorophenyl)-butyric acid; (R)-3-amino-4-(3-methylphenyl)-butyric acid; (R)-3-amino-4-(3-pyridyl)-butyric acid; (R)-3-amino-4-(3-thienyl)-butyric acid; (R)-3-amino-4-(3-trifluoromethylphenyl)-butyric acid; (R)-3-amino-4-(4-bromophenyl)-butyric acid; (R)-3-amino-4-(4-chlorophenyl)-butyric acid; (R)-3-amino-4-(4-cyanophenyl)-butyric acid; (R)-3-amino-4-(4-fluorophenyl)-butyric acid; (R)-3-amino-4-(4-iodophenyl)-butyric acid; (R)-3-amino-4-(4-methylphenyl)-butyric acid; (R)-3-amino-4-(4-nitrophenyl)-butyric acid; (R)-3-amino-4-(4-pyridyl)-butyric acid; (R)-3-amino-4-(4-trifluoromethylphenyl)-butyric acid; (R)-3-amino-4-pentafluoro-phenylbutyric acid; (R)-3-amino-5-hexenoic acid; (R)-3-amino-5-hexynoic acid; (R)-3-amino-5-phenylpentanoic acid; (R)-3-amino-6-phenyl-5-hexenoic acid; (S)-1,2,3,4-tetrahydro-isoquinoline-3-acetic acid; (S)-3-amino-4-(1-naphthyl)-butyric acid; (S)-3-amino-4-(2,4-dichlorophenyl)butyric acid; (S)-3-amino-4-(2-chlorophenyl)-butyric acid; (S)-3-amino-4-(2-cyanophenyl)-butyric acid; (S)-3-amino-4-(2-fluorophenyl)-butyric acid; (S)-3-amino-4-(2-furyl)-butyric acid; (S)-3-amino-4-(2-methylphenyl)-butyric acid; (S)-3-amino-4-(2-naphthyl)-butyric acid; (S)-3-amino-4-(2-thienyl)-butyric acid; (S)-3-amino-4-(2-trifluoromethylphenyl)-butyric acid; (S)-3-amino-4-(3,4-dichlorophenyl)butyric acid; (S)-3-amino-4-(3,4-difluorophenyl)butyric acid; (S)-3-amino-4-(3-benzothienyl)-butyric acid; (S)-3-amino-4-(3-chlorophenyl)-butyric acid; (S)-3-amino-4-(3-cyanophenyl)-butyric acid; (S)-3-amino-4-(3-fluorophenyl)-butyric acid; (S)-3-amino-4-(3-methylphenyl)-butyric acid; (S)-3-amino-4-(3-pyridyl)-butyric acid; (S)-3-amino-4-(3-thienyl)-butyric acid; (S)-3-amino-4-(3-trifluoromethylphenyl)-butyric acid; (S)-3-amino-4-(4-bromophenyl)-butyric acid; (S)-3-amino-4-(4-chlorophenyl)-butyric acid; (S)-3-amino-4-(4-cyanophenyl)-butyric acid; (S)-3-amino-4-(4-fluorophenyl)-butyric acid; (S)-3-amino-4-(4-iodophenyl)-butyric acid; (S)-3-amino-4-(4-methylphenyl)-butyric acid; (S)-3-amino-4-(4-nitrophenyl)-butyric acid; (S)-3-amino-4-(4-pyridyl)-butyric acid; (S)-3-amino-4-(4-trifluoromethylphenyl)-butyric acid; (S)-3-amino-4-pentafluoro-phenylbutyric acid; (S)-3-amino-5-hexenoic acid; (S)-3-amino-5-hexynoic acid; (S)-3-amino-5-phenylpentanoic acid; (S)-3-amino-6-phenyl-5-hexenoic acid; 1,2,5,6-tetrahydropyridine-3-carboxylic acid; 1,2,5,6-tetrahydropyridine-4-carboxylic acid; 3-amino-3-(2-chlorophenyl)-propionic acid; 3-amino-3-(2-thienyl)-propionic acid; 3-amino-3-(3-bromophenyl)-propionic acid; 3-amino-3-(4-chlorophenyl)-propionic acid; 3-amino-3-(4-methoxyphenyl)-propionic acid; 3-amino-4,4,4-trifluoro-butyric acid; 3-aminoadipic acid; D-β-phenylalanine; β-leucine; L-β-homoalanine; L-β-homoaspartic acid γ-benzyl ester; L-β-homoglutamic acid 6-benzyl ester; L-β-homoisoleucine; L-β-homoleucine; L-β-homomethionine; L-β-homophenylalanine; L-β-homoproline; L-β-homotryptophan; L-β-homovaline; L-Nω-benzyloxycarbonyl-β-homolysine; Nω-L-β-homoarginine; O-benzyl-L-β-homohydroxyproline; O-benzyl-L-β-homoserine; O-benzyl-L-β-homothreonine; O-benzyl-L-β-homotyrosine; γ-trityl-L-β-homoasparagine; (R)-β-phenylalanine; L-β-homoaspartic acid γ-t-butyl ester; L-β-homoglutamic acid δ-t-butyl ester; L-Nω-β-homolysine; Nδ-trityl-L-β-homoglutamine; Nω-2,2,4,6,7-pentamethyl-dihydrobenzofuran-5-sulfonyl-L-β-homoarginine; O-t-butyl-L-β-homohydroxy-proline; O-t-butyl-L-β-homoserine; O-t-butyl-L-β-homothreonine; O-t-butyl-L-β-homotyrosine; 2-aminocyclopentane carboxylic acid; and 2-aminocyclohexane carboxylic acid.

Amino acid analogs include analogs of alanine, valine, glycine or leucine. Examples of amino acid analogs of alanine, valine, glycine, and leucine include, but are not limited to, the following: α-methoxyglycine; α-allyl-L-alanine; α-aminoisobutyric acid; α-methyl-leucine; β-(1-naphthyl)-D-alanine; β-(1-naphthyl)-L-alanine; β-(2-naphthyl)-D-alanine; β-(2-naphthyl)-L-alanine; β-(2-pyridyl)-D-alanine; β-(2-pyridyl)-L-alanine; β-(2-thienyl)-D-alanine; β-(2-thienyl)-L-alanine; β-(3-benzothienyl)-D-alanine; β-(3-benzothienyl)-L-alanine; β-(3-pyridyl)-D-alanine; β-(3-pyridyl)-L-alanine; β-(4-pyridyl)-D-alanine; β-(4-pyridyl)-L-alanine; β-chloro-L-alanine; β-cyano-L-alanin; β-cyclohexyl-D-alanine; β-cyclohexyl-L-alanine; β-cyclopenten-1-yl-alanine; β-cyclopentyl-alanine; β-cyclopropyl-L-Ala-OH. dicyclohexylammonium salt; β-t-butyl-D-alanine; β-t-butyl-L-alanine; γ-aminobutyric acid; L-α,β-diaminopropionic acid; 2,4-dinitro-phenylglycine; 2,5-dihydro-D-phenylglycine; 2-amino-4,4,4-trifluorobutyric acid; 2-fluoro-phenylglycine; 3-amino-4,4,4-trifluoro-butyric acid; 3-fluoro-valine; 4,4,4-trifluoro-valine; 4,5-dehydro-L-leu-OH.dicyclohexylammonium salt; 4-fluoro-D-phenylglycine; 4-fluoro-L-phenylglycine; 4-hydroxy-D-phenylglycine; 5,5,5-trifluoro-leucine; 6-aminohexanoic acid; cyclopentyl-D-Gly-OH.dicyclohexylammonium salt; cyclopentyl-Gly-OH.dicyclohexylammonium salt; D-α,β-diaminopropionic acid; D-α-aminobutyric acid; D-α-t-butylglycine; D-(2-thienyl)glycine; D-(3-thienyl)glycine; D-2-aminocaproic acid; D-2-indanylglycine; D-allylglycine.dicyclohexylammonium salt; D-cyclohexylglycine; D-norvaline; D-phenylglycine; β-aminobutyric acid; β-aminoisobutyric acid; (2-bromophenyl)glycine; (2-methoxyphenyl)glycine; (2-methylphenyl)glycine; (2-thiazoyl)glycine; (2-thienyl)glycine; 2-amino-3-(dimethylamino)-propionic acid; L-α,β-diaminopropionic acid; L-α-aminobutyric acid; L-α-t-butylglycine; L-(3-thienyl)glycine; L-2-amino-3-(dimethylamino)-propionic acid; L-2-aminocaproic acid dicyclohexyl-ammonium salt; L-2-indanylglycine; L-allylglycine.dicyclohexyl ammonium salt; L-cyclohexylglycine; L-phenylglycine; L-propargylglycine; L-norvaline; N-α-aminomethyl-L-alanine; D-α,γ-diaminobutyric acid; L-α,γ-diaminobutyric acid; β-cyclopropyl-L-alanine; (N-β-(2,4-dinitrophenyl))-L-α,β-diaminopropionic acid; (N-β-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl)-D-α,β-diaminopropionic acid; (N-β-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl)-L-α,β-diaminopropionic acid; (N-β-4-methyltrityl)-L-α,β-diaminopropionic acid; (N-β-allyloxycarbonyl)-L-α,β-diaminopropionic acid; (N-γ-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl)-D-α,γ-diaminobutyric acid; (N-γ-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl)-L-α,γ-diaminobutyric acid; (N-γ-4-methyltrityl)-D-α,γ-diaminobutyric acid; (N-γ-4-methyltrityl)-L-α,γ-diaminobutyric acid; (N-γ-allyloxycarbonyl)-L-α,γ-diaminobutyric acid; D-α,γ-diaminobutyric acid; 4,5-dehydro-L-leucine; cyclopentyl-D-Gly-OH; cyclopentyl-Gly-OH; D-allylglycine; D-homocyclohexylalanine; L-1-pyrenylalanine; L-2-aminocaproic acid; L-allylglycine; L-homocyclohexylalanine; and N-(2-hydroxy-4-methoxy-Bzl)-Gly-OH.

Amino acid analogs include analogs of arginine or lysine. Examples of amino acid analogs of arginine and lysine include, but are not limited to, the following: citrulline; L-2-amino-3-guanidinopropionic acid; L-2-amino-3-ureidopropionic acid; L-citrulline; Lys(Me)₂-OH; Lys(N₃)—OH; Nδ-benzyloxycarbonyl-L-ornithine; Nω-nitro-D-arginine; Nω-nitro-L-arginine; α-methyl-ornithine; 2,6-diaminoheptanedioic acid; L-ornithine; (Nδ-1-(4,4-dimethyl-2,6-dioxo-cyclohex-1-ylidene)ethyl)-D-ornithine; (Nδ-1-(4,4-dimethyl-2,6-dioxo-cyclohex-1-ylidene)ethyl)-L-ornithine; (Nδ-4-methyltrityl)-D-ornithine; (Nδ-4-methyltrityl)-L-ornithine; D-ornithine; L-ornithine; Arg(Me)(Pbf)-OH; Arg(Me)₂-OH (asymmetrical); Arg(Me)2-OH (symmetrical); Lys(ivDde)-OH; Lys(Me)2-OH.HCl; Lys(Me3)-OH chloride; Nω-nitro-D-arginine; and Nω-nitro-L-arginine.

Amino acid analogs include analogs of aspartic or glutamic acids. Examples of amino acid analogs of aspartic and glutamic acids include, but are not limited to, the following: α-methyl-D-aspartic acid; α-methyl-glutamic acid; α-methyl-L-aspartic acid; γ-methylene-glutamic acid; (N-γ-ethyl)-L-glutamine; [N-α-(4-aminobenzoyl)]-L-glutamic acid; 2,6-diaminopimelic acid; L-α-aminosuberic acid; D-2-aminoadipic acid; D-α-aminosuberic acid; α-aminopimelic acid; iminodiacetic acid; L-2-aminoadipic acid; threo-β-methyl-aspartic acid; γ-carboxy-D-glutamic acid γ,γ-di-t-butyl ester; γ-carboxy-L-glutamic acid γ,γ-di-t-butyl ester; Glu(OAll)-OH; L-Asu(OtBu)-OH; and pyroglutamic acid.

Amino acid analogs include analogs of cysteine and methionine. Examples of amino acid analogs of cysteine and methionine include, but are not limited to, Cys(farnesyl)-OH, Cys(farnesyl)-OMe, α-methyl-methionine, Cys(2-hydroxyethyl)-OH, Cys(3-aminopropyl)-OH, 2-amino-4-(ethylthio)butyric acid, buthionine, buthioninesulfoximine, ethionine, methionine methylsulfonium chloride, selenomethionine, cysteic acid, [2-(4-pyridyl)ethyl]-DL-penicillamine, [2-(4-pyridyl)ethyl]-L-cysteine, 4-methoxybenzyl-D-penicillamine, 4-methoxybenzyl-L-penicillamine, 4-methylbenzyl-D-penicillamine, 4-methylbenzyl-L-penicillamine, benzyl-D-cysteine, benzyl-L-cysteine, benzyl-DL-homocysteine, carbamoyl-L-cysteine, carboxyethyl-L-cysteine, carboxymethyl-L-cysteine, diphenylmethyl-L-cysteine, ethyl-L-cysteine, methyl-L-cysteine, t-butyl-D-cysteine, trityl-L-homocysteine, trityl-D-penicillamine, cystathionine, homocystine, L-homocystine, (2-aminoethyl)-L-cysteine, seleno-L-cystine, cystathionine, Cys(StBu)-OH, and acetamidomethyl-D-penicillamine

Amino acid analogs include analogs of phenylalanine and tyrosine. Examples of amino acid analogs of phenylalanine and tyrosine include β-methyl-phenylalanine, β-hydroxyphenylalanine, α-methyl-3-methoxy-DL-phenylalanine, α-methyl-D-phenylalanine, α-methyl-L-phenylalanine, 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, 2,4-dichloro-phenylalanine, 2-(trifluoromethyl)-D-phenylalanine, 2-(trifluoromethyl)-L-phenylalanine, 2-bromo-D-phenylalanine, 2-bromo-L-phenylalanine, 2-chloro-D-phenylalanine, 2-chloro-L-phenylalanine, 2-cyano-D-phenylalanine, 2-cyano-L-phenylalanine, 2-fluoro-D-phenylalanine, 2-fluoro-L-phenylalanine, 2-methyl-D-phenylalanine, 2-methyl-L-phenylalanine, 2-nitro-D-phenylalanine, 2-nitro-L-phenylalanine, 2;4;5-trihydroxy-phenylalanine, 3,4,5-trifluoro-D-phenylalanine, 3,4,5-trifluoro-L-phenylalanine, 3,4-dichloro-D-phenylalanine, 3,4-dichloro-L-phenylalanine, 3,4-difluoro-D-phenylalanine, 3,4-difluoro-L-phenylalanine, 3,4-dihydroxy-L-phenylalanine, 3,4-dimethoxy-L-phenylalanine, 3,5,3′-triiodo-L-thyronine, 3,5-diiodo-D-tyrosine, 3,5-diiodo-L-tyrosine, 3,5-diiodo-L-thyronine, 3-(trifluoromethyl)-D-phenylalanine, 3-(trifluoromethyl)-L-phenylalanine, 3-amino-L-tyrosine, 3-bromo-D-phenylalanine, 3-bromo-L-phenylalanine, 3-chloro-D-phenylalanine, 3-chloro-L-phenylalanine, 3-chloro-L-tyrosine, 3-cyano-D-phenylalanine, 3-cyano-L-phenylalanine, 3-fluoro-D-phenylalanine, 3-fluoro-L-phenylalanine, 3-fluoro-tyrosine, 3-iodo-D-phenylalanine, 3-iodo-L-phenylalanine, 3-iodo-L-tyrosine, 3-methoxy-L-tyrosine, 3-methyl-D-phenylalanine, 3-methyl-L-phenylalanine, 3-nitro-D-phenylalanine, 3-nitro-L-phenylalanine, 3-nitro-L-tyrosine, 4-(trifluoromethyl)-D-phenylalanine, 4-(trifluoromethyl)-L-phenylalanine, 4-amino-D-phenylalanine, 4-amino-L-phenylalanine, 4-benzoyl-D-phenylalanine, 4-benzoyl-L-phenylalanine, 4-bis(2-chloroethyl)amino-L-phenylalanine, 4-bromo-D-phenylalanine, 4-bromo-L-phenylalanine, 4-chloro-D-phenylalanine, 4-chloro-L-phenylalanine, 4-cyano-D-phenylalanine, 4-cyano-L-phenylalanine, 4-fluoro-D-phenylalanine, 4-fluoro-L-phenylalanine, 4-iodo-D-phenylalanine, 4-iodo-L-phenylalanine, homophenylalanine, thyroxine, 3,3-diphenylalanine, thyronine, ethyl-tyrosine, and methyl-tyrosine.

Amino acid analogs include analogs of proline. Examples of amino acid analogs of proline include, but are not limited to, 3,4-dehydro-proline, 4-fluoro-proline, cis-4-hydroxy-proline, thiazolidine-2-carboxylic acid, and trans-4-fluoro-proline.

Amino acid analogs include analogs of serine and threonine. Examples of amino acid analogs of serine and threonine include, but are not limited to, 3-amino-2-hydroxy-5-methylhexanoic acid, 2-amino-3-hydroxy-4-methylpentanoic acid, 2-amino-3-ethoxybutanoic acid, 2-amino-3-methoxybutanoic acid, 4-amino-3-hydroxy-6-methylheptanoic acid, 2-amino-3-benzyloxypropionic acid, 2-amino-3-benzyloxypropionic acid, 2-amino-3-ethoxypropionic acid, 4-amino-3-hydroxybutanoic acid, and α-methylserine.

Amino acid analogs include analogs of tryptophan. Examples of amino acid analogs of tryptophan include, but are not limited to, the following: α-methyl-tryptophan; β-(3-benzothienyl)-D-alanine; β-(3-benzothienyl)-L-alanine; 1-methyl-tryptophan; 4-methyl-tryptophan; 5-benzyloxy-tryptophan; 5-bromo-tryptophan; 5-chloro-tryptophan; 5-fluoro-tryptophan; 5-hydroxy-tryptophan; 5-hydroxy-L-tryptophan; 5-methoxy-tryptophan; 5-methoxy-L-tryptophan; 5-methyl-tryptophan; 6-bromo-tryptophan; 6-chloro-D-tryptophan; 6-chloro-tryptophan; 6-fluoro-tryptophan; 6-methyl-tryptophan; 7-benzyloxy-tryptophan; 7-bromo-tryptophan; 7-methyl--tryptophan; D-1,2,3,4-tetrahydro-norharman-3-carboxylic acid; 6-methoxy-1,2,3,4-tetrahydronorharman-1-carboxylic acid; 7-azatryptophan; L-1,2,3,4-tetrahydro-norharman-3-carboxylic acid; 5-methoxy-2-methyl-tryptophan; and 6-chloro-L-tryptophan.

In some embodiments, amino acid analogs are racemic. In some embodiments, the D isomer of the amino acid analog is used. In some embodiments, the L isomer of the amino acid analog is used. In other embodiments, the amino acid analog comprises chiral centers that are in the R or S configuration. In still other embodiments, the amino group(s) of a β-amino acid analog is substituted with a protecting group, e.g., tert-butyloxycarbonyl (BOC group), 9-fluorenylmethyloxycarbonyl (FMOC), tosyl, and the like. In yet other embodiments, the carboxylic acid functional group of a β-amino acid analog is protected, e.g., as its ester derivative. In some embodiments the salt of the amino acid analog is used.

A “non-essential” amino acid residue is a residue that can be altered from the wild-type sequence of a polypeptide without abolishing or substantially altering its essential biological or biochemical activity (e.g., receptor binding or activation). An “essential” amino acid residue is a residue that, when altered from the wild-type sequence of the polypeptide, results in abolishing or substantially abolishing the polypeptide's essential biological or biochemical activity.

A “conservative amino acid substitution” is one in which the amino acid residue is replaced with an amino acid residue having a similar side chain. Families of amino acid residues having similar side chains have been defined in the art. These families include amino acids with basic side chains (e.g., K, R, H), acidic side chains (e.g., D, E), uncharged polar side chains (e.g., G, N, Q, S, T, Y, C), nonpolar side chains (e.g., A, V, L, I, P, F, M, W), beta-branched side chains (e.g., T, V, I) and aromatic side chains (e.g., Y, F, W, H). Thus, a predicted nonessential amino acid residue in a polypeptide, for example, is replaced with another amino acid residue from the same side chain family. Other examples of acceptable substitutions are substitutions based on isosteric considerations (e.g. norleucine for methionine) or other properties (e.g. 2-thienylalanine for phenylalanine, or 6-Cl-tryptophan for tryptophan).

The term “capping group” refers to the chemical moiety occurring at either the carboxy or amino terminus of the polypeptide chain of the subject peptidomimetic macrocycle. The capping group of a carboxy terminus includes an unmodified carboxylic acid (i.e. —COOH) or a carboxylic acid with a substituent. For example, the carboxy terminus can be substituted with an amino group to yield a carboxamide at the C-terminus. Various substituents include but are not limited to primary and secondary amines, including pegylated secondary amines Representative secondary amine capping groups for the C-terminus include:

The capping group of an amino terminus includes an unmodified amine (ie —NH₂) or an amine with a substituent. For example, the amino terminus can be substituted with an acyl group to yield a carboxamide at the N-terminus. Various substituents include but are not limited to substituted acyl groups, including C₁-C₆ carbonyls, C₇-C₃₀ carbonyls, and pegylated carbamates. Representative capping groups for the N-terminus include, but are not limited to, 4-FBzl (4-fluoro-benzyl) and the following:

The term “member” as used herein in conjunction with macrocycles or macrocycle-forming linkers refers to the atoms that form or can form the macrocycle, and excludes substituent or side chain atoms. By analogy, cyclodecane, 1,2-difluoro-decane and 1,3-dimethyl cyclodecane are all considered ten-membered macrocycles as the hydrogen or fluoro substituents or methyl side chains do not participate in forming the macrocycle.

The symbol “

” when used as part of a molecular structure refers to a single bond or a trans or cis double bond.

The term “amino acid side chain” refers to a moiety attached to the α-carbon (or another backbone atom) in an amino acid. For example, the amino acid side chain for alanine is methyl, the amino acid side chain for phenylalanine is phenylmethyl, the amino acid side chain for cysteine is thiomethyl, the amino acid side chain for aspartate is carboxymethyl, the amino acid side chain for tyrosine is 4-hydroxyphenylmethyl, etc. Other non-naturally occurring amino acid side chains are also included, for example, those that occur in nature (e.g., an amino acid metabolite) or those that are made synthetically (e.g., an α,α di-substituted amino acid).

The term “α,α di-substituted amino” acid refers to a molecule or moiety containing both an amino group and a carboxyl group bound to a carbon (the α-carbon) that is attached to two natural or non-natural amino acid side chains.

The term “polypeptide” encompasses two or more naturally or non-naturally-occurring amino acids joined by a covalent bond (e.g., an amide bond). Polypeptides as described herein include full length proteins (e.g., fully processed proteins) as well as shorter amino acid sequences (e.g., fragments of naturally-occurring proteins or synthetic polypeptide fragments).

The term “first C-terminal amino acid” refers to the amino acid which is closest to the C-terminus. The term “second C-terminal amino acid” refers to the amino acid attached at the N-terminus of the first C-terminal amino acid.

The term “macrocyclization reagent” or “macrocycle-forming reagent” as used herein refers to any reagent which can be used to prepare a peptidomimetic macrocycle by mediating the reaction between two reactive groups. Reactive groups can be, for example, an azide and alkyne, in which case macrocyclization reagents include, without limitation, Cu reagents such as reagents which provide a reactive Cu(I) species, such as CuBr, CuI or CuOTf, as well as Cu(II) salts such as Cu(CO₂CH₃)₂, CuSO₄, and CuCl₂ that can be converted in situ to an active Cu(I) reagent by the addition of a reducing agent such as ascorbic acid or sodium ascorbate. Macrocyclization reagents can additionally include, for example, Ru reagents known in the art such as Cp*RuCl(PPh₃)₂, [Cp*RuCl]₄ or other Ru reagents which can provide a reactive Ru(II) species. In other cases, the reactive groups are terminal olefins. In such embodiments, the macrocyclization reagents or macrocycle-forming reagents are metathesis catalysts including, but not limited to, stabilized, late transition metal carbene complex catalysts such as Group VIII transition metal carbene catalysts. For example, such catalysts are Ru and Os metal centers having a +2 oxidation state, an electron count of 16 and pentacoordinated. In other examples, catalysts have W or Mo centers. Various catalysts are disclosed in Grubbs et al., “Ring Closing Metathesis and Related Processes in Organic Synthesis” Acc. Chem. Res. 1995, 28, 446-452, U.S. Pat. No. 5,811,515; U.S. Pat. No. 7,932,397; U.S. Application No. 2011/0065915; U.S. Application No. 2011/0245477; Yu et al., “Synthesis of Macrocyclic Natural Products by Catalyst-Controlled Stereoselective Ring-Closing Metathesis,” Nature 2011, 479, 88; and Peryshkov et al., “Z-Selective Olefin Metathesis Reactions Promoted by Tungsten Oxo Alkylidene Complexes,” J. Am. Chem. Soc. 2011, 133, 20754. In yet other cases, the reactive groups are thiol groups. In such embodiments, the macrocyclization reagent is, for example, a linker functionalized with two thiol-reactive groups such as halogen groups. In some examples, the macrocyclization reagent include palladium reagents, for example Pd(PPh₃)₄, Pd(PPh₃)₂Cl₂, Pd(dppe)Cl, Pd(dppp)Cl₂, and Pd(dppf)Cl₂.

The term “halo” or “halogen” refers to fluorine, chlorine, bromine or iodine or a radical thereof.

The term “alkyl” refers to a hydrocarbon chain that is a straight chain or branched chain, containing the indicated number of carbon atoms. For example, C₁-C₁₀ indicates that the group has from 1 to 10 (inclusive) carbon atoms in it. In the absence of any numerical designation, “alkyl” is a chain (straight or branched) having 1 to 20 (inclusive) carbon atoms in it.

The term “alkylene” refers to a divalent alkyl (i.e., —R—).

The term “alkenyl” refers to a hydrocarbon chain that is a straight chain or branched chain having one or more carbon-carbon double bonds. The alkenyl moiety contains the indicated number of carbon atoms. For example, C₂-C₁₀ indicates that the group has from 2 to 10 (inclusive) carbon atoms in it. The term “lower alkenyl” refers to a C₂-C₆ alkenyl chain. In the absence of any numerical designation, “alkenyl” is a chain (straight or branched) having 2 to 20 (inclusive) carbon atoms in it.

The term “alkynyl” refers to a hydrocarbon chain that is a straight chain or branched chain having one or more carbon-carbon triple bonds. The alkynyl moiety contains the indicated number of carbon atoms. For example, C₂-C₁₀ indicates that the group has from 2 to 10 (inclusive) carbon atoms in it. The term “lower alkynyl” refers to a C₂-C₆ alkynyl chain. In the absence of any numerical designation, “alkynyl” is a chain (straight or branched) having 2 to 20 (inclusive) carbon atoms in it.

The term “aryl” refers to a 6-carbon monocyclic or 10-carbon bicyclic aromatic ring system wherein 0, 1, 2, 3, or 4 atoms of each ring are substituted by a substituent. Examples of aryl groups include phenyl, naphthyl and the like. The term “arylalkoxy” refers to an alkoxy substituted with aryl.

“Arylalkyl” refers to an aryl group, as defined above, wherein one of the aryl group's hydrogen atoms has been replaced with a C₁-C₅ alkyl group, as defined above. Representative examples of an arylalkyl group include, but are not limited to, 2-methylphenyl, 3-methylphenyl, 4-methylphenyl, 2-ethylphenyl, 3-ethylphenyl, 4-ethylphenyl, 2-propylphenyl, 3-propylphenyl, 4-propylphenyl, 2-butylphenyl, 3-butylphenyl, 4-butylphenyl, 2-pentylphenyl, 3-pentylphenyl, 4-pentylphenyl, 2-isopropylphenyl, 3-isopropylphenyl, 4-isopropylphenyl, 2-isobutylphenyl, 3-isobutylphenyl, 4-isobutylphenyl, 2-sec-butylphenyl, 3-sec-butylphenyl, 4-sec-butylphenyl, 2-t-butylphenyl, 3-t-butylphenyl and 4-t-butylphenyl.

“Arylamido” refers to an aryl group, as defined above, wherein one of the aryl group's hydrogen atoms has been replaced with one or more —C(O)NH₂ groups. Representative examples of an arylamido group include 2-C(O)NH₂-phenyl, 3-C(O)NH₂-phenyl, 4-C(O)NH₂-phenyl, 2-C(O)NH₂-pyridyl, 3-C(O)NH₂-pyridyl, and 4-C(O)NH₂-pyridyl,

“Alkylheterocycle” refers to a C₁-C₅ alkyl group, as defined above, wherein one of the C₁-C₅ alkyl group's hydrogen atoms has been replaced with a heterocycle. Representative examples of an alkylheterocycle group include, but are not limited to, —CH₂CH₂-morpholine, —CH₂CH₂-piperidine, —CH₂CH₂CH₂-morpholine, and —CH₂CH₂CH₂-imidazole.

“Alkylamido” refers to a C₁-C₅ alkyl group, as defined above, wherein one of the C₁-C₅ alkyl group's hydrogen atoms has been replaced with a —C(O)NH₂ group. Representative examples of an alkylamido group include, but are not limited to, —CH₂—C(O)NH₂, —CH₂CH₂—C(O)NH₂, —CH₂CH₂CH₂C(O)NH₂, —CH₂CH₂CH₂CH₂C(O)NH₂, —CH₂CH₂CH₂CH₂CH₂C(O)NH₂, —CH₂CH(C(O)NH₂)CH₃, —CH₂CH(C(O)NH₂)CH₂CH₃, —CH(C(O)NH₂)CH₂CH₃, —C(CH₃)₂CH₂C(O)NH₂, —CH₂—CH₂—NH—C(O)—CH₃, —CH₂—CH₂—NH—C(O)—CH₃—CH3, and —CH₂—CH₂—NH—C(O)—CH═CH₂.

“Alkanol” refers to a C₁-C₅ alkyl group, as defined above, wherein one of the C₁-C₅ alkyl group's hydrogen atoms has been replaced with a hydroxyl group. Representative examples of an alkanol group include, but are not limited to, —CH₂OH, —CH₂CH₂OH, —CH₂CH₂CH₂OH, —CH₂CH₂CH₂CH₂OH, —CH₂CH₂CH₂CH₂CH₂OH, —CH₂CH(OH)CH₃, —CH₂CH(OH)CH₂CH₃, —CH(OH)CH₃ and —C(CH₃)₂CH₂OH.

“Alkylcarboxy” refers to a C₁-C₅ alkyl group, as defined above, wherein one of the C₁-C₅ alkyl group's hydrogen atoms has been replaced with a —COOH group. Representative examples of an alkylcarboxy group include, but are not limited to, —CH₂COOH, —CH₂CH₂COOH, —CH₂CH₂CH₂COOH, —CH₂CH₂CH₂CH₂COOH, —CH₂CH(COOH)CH₃, —CH₂CH₂CH₂CH₂CH₂COOH, —CH₂CH(COOH)CH₂CH₃, —CH(COOH)CH₂CH₃ and —C(CH₃)₂CH₂COOH.

The term “cycloalkyl” as employed herein includes saturated and partially unsaturated cyclic hydrocarbon groups having 3 to 12 carbons, preferably 3 to 8 carbons, and more preferably 3 to 6 carbons, wherein the cycloalkyl group additionally is optionally substituted. Some cycloalkyl groups include, without limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, and cyclooctyl.

The term “heteroaryl” refers to an aromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of O, N, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2, 3, or 4 atoms of each ring are substituted by a substituent. Examples of heteroaryl groups include pyridyl, furyl or furanyl, imidazolyl, benzimidazolyl, pyrimidinyl, thiophenyl or thienyl, quinolinyl, indolyl, thiazolyl, and the like.

The term “heteroarylalkyl” or the term “heteroaralkyl” refers to an alkyl substituted with a heteroaryl. The term “heteroarylalkoxy” refers to an alkoxy substituted with heteroaryl.

The term “heteroarylalkyl” or the term “heteroaralkyl” refers to an alkyl substituted with a heteroaryl. The term “heteroarylalkoxy” refers to an alkoxy substituted with heteroaryl.

The term “heterocyclyl” refers to a nonaromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of O, N, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2 or 3 atoms of each ring are substituted by a substituent. Examples of heterocyclyl groups include piperazinyl, pyrrolidinyl, dioxanyl, morpholinyl, tetrahydrofuranyl, and the like.

The term “substituent” refers to a group replacing a second atom or group such as a hydrogen atom on any molecule, compound or moiety. Suitable substituents include, without limitation, halo, hydroxy, mercapto, oxo, nitro, haloalkyl, alkyl, alkaryl, aryl, aralkyl, alkoxy, thioalkoxy, aryloxy, amino, alkoxycarbonyl, amido, carboxy, alkanesulfonyl, alkylcarbonyl, and cyano groups.

In some embodiments, the compounds disclosed herein contain one or more asymmetric centers and thus occur as racemates and racemic mixtures, single enantiomers, individual diastereomers and diastereomeric mixtures. All such isomeric forms of these compounds are included unless expressly provided otherwise. In some embodiments, the compounds disclosed herein are also represented in multiple tautomeric forms, in such instances, the compounds include all tautomeric forms of the compounds described herein (e.g., if alkylation of a ring system results in alkylation at multiple sites, the disclosure includes all such reaction products). All such isomeric forms of such compounds are included unless expressly provided otherwise. All crystal forms of the compounds described herein are included unless expressly provided otherwise.

As used herein, the terms “increase” and “decrease” mean, respectively, to cause a statistically significantly (i.e., p<0.1) increase or decrease of at least 5%.

As used herein, the recitation of a numerical range for a variable is intended to convey that the variable is equal to any of the values within that range. Thus, for a variable which is inherently discrete, the variable is equal to any integer value within the numerical range, including the end-points of the range. Similarly, for a variable which is inherently continuous, the variable is equal to any real value within the numerical range, including the end-points of the range. As an example, and without limitation, a variable which is described as having values between 0 and 2 takes the values 0, 1 or 2 if the variable is inherently discrete, and takes the values 0.0, 0.1, 0.01, 0.001, or any other real values ≧0 and ≦2 if the variable is inherently continuous.

As used herein, unless specifically indicated otherwise, the word “or” is used in the inclusive sense of “and/or” and not the exclusive sense of “either/or.”

The term “on average” represents the mean value derived from performing at least three independent replicates for each data point.

The term “biological activity” encompasses structural and functional properties of a macrocycle.

Biological activity is, for example, structural stability, alpha-helicity, affinity for a target, resistance to proteolytic degradation, cell penetrability, intracellular stability, in vivo stability, or any combination thereof.

The term “binding affinity” refers to the strength of a binding interaction, for example between a peptidomimetic macrocycle and a target. Binding affinity can be expressed, for example, as an equilibrium dissociation constant (“K_(D)”), which is expressed in units which are a measure of concentration (e.g. M, mM, μM, nM etc). Numerically, binding affinity and K_(D) values vary inversely, such that a lower binding affinity corresponds to a higher K_(D) value, while a higher binding affinity corresponds to a lower K_(D) value. Where high binding affinity is desirable, “improved” binding affinity refers to higher binding affinity and therefore lower K_(D) values.

The term “in vitro efficacy” refers to the extent to which a test compound, such as a peptidomimetic macrocycle, produces a beneficial result in an in vitro test system or assay. In vitro efficacy can be measured, for example, as an “IC₅₀” or “EC₅₀” value, which represents the concentration of the test compound which produces 50% of the maximal effect in the test system.

The term “ratio of in vitro efficacies” or “in vitro efficacy ratio” refers to the ratio of IC₅₀ or EC₅₀ values from a first assay (the numerator) versus a second assay (the denominator). Consequently, an improved in vitro efficacy ratio for Assay 1 versus Assay 2 refers to a lower value for the ratio expressed as IC₅₀(Assay 1)/IC₅₀(Assay 2) or alternatively as EC₅₀(Assay 1)/EC₅₀(Assay 2). This concept can also be characterized as “improved selectivity” in Assay 1 versus Assay 2, which can be due either to a decrease in the IC₅₀ or EC₅₀ value for Target 1 or an increase in the value for the IC₅₀ or EC₅₀ value for Target 2.

The term “solid tumor” or “solid cancer” as used herein refers to tumors that usually do not contain cysts or liquid areas. Solid tumors as used herein include sarcomas, carcinomas and lymphomas. In various embodiments leukemia (cancer of blood) is not solid tumor.

The term “adverse event” (AE) as used herein includes any noxious, pathological, or unintended change in anatomical, physiological, or metabolic functions as indicated by physical signs, symptoms, and/or laboratory changes occurring in any phase of the clinical study whether or not temporally associated with the administration of study medication and whether or not considered related to the study medication. This definition includes an exacerbation of pre-existing medical conditions or events, intercurrent illnesses, hypersensitivity reactions, drug interactions, or clinically significant laboratory findings. An AE does not include the following: (i) medical or surgical procedures, e.g., tooth extraction, transfusion, surgery (The medical condition that leads to the procedure is to be recorded as an AE); (ii) pre-existing conditions or procedures present or detected at the start of the study that do not worsen; (iii) hospitalization for elective surgeries or for other situations in which an untoward medical event has not occurred; (iv) abnormal laboratory value, unless it is clinically significant according to the Investigator, requires intervention, or results in a delay, discontinuation or change in the dose of study drug; (v) overdose of study drug or concomitant medication unaccompanied by signs/symptoms; if sign/symptoms occur, the final diagnosis should be recorded as an AE; (vi) pregnancy by itself, unless a complication occurs during pregnancy leading to hospitalization; in this case, the medical condition that leads to the hospitalization is to be recorded as the AE; and (vii) significant worsening of the disease under investigation which is captured as an efficacy parameter in this study and, thus, is not recorded as an AE.

The term serious adverse event (SAE) as used herein refers to an adverse event that results in any of the following outcomes: (i) death; (ii) life-threatening adverse experience (i e, immediate risk of death from the event as it occurred; this does not include an adverse event that, had it occurred in a more serious form, might have caused death); (iii) persistent or significant disability/incapacitation; (iv) hospitalization or prolongation of existing hospitalization; and (v) congenital anomaly/birth defect. Important medical events that may not result in death, be life-threatening, or require hospitalization can be considered serious when, based on medical judgment, they can jeopardize the patient or may require medical or surgical intervention to prevent one of the outcomes listed in this definition. Hospitalizations due to the underlying disease will not be reported as an SAE unless there is reason to suspect a causal relationship with the study drug.

An AE or suspected adverse reaction is considered “unexpected” (referred to as Unexpected Adverse Event (UAE) if it is not listed in the peptidomimetic macrocycle Investigator's Brochure or is not listed at the specificity or severity that has been observed; or, is not consistent with the risk information described in the protocol or elsewhere. For example, under this definition, hepatic necrosis would be unexpected (by virtue of greater severity) if the Investigator's Brochure referred only to elevated hepatic enzymes or hepatitis. Similarly, cerebral thromboembolism and cerebral vasculitis would be unexpected (by virtue of greater specificity) if the Investigator's Brochure listed only cerebral vascular accidents. “Unexpected,” as used in this definition, also refers to AEs or suspected adverse reactions that are mentioned in the Investigator's Brochure as occurring with a class of drugs or as anticipated from the pharmacological properties of the peptidomimetic macrocycle but are not specifically mentioned as occurring with the peptidomimetic macrocycle.

A “Dose-Limiting Toxicity” (DLT) as used herein is defined as any Grade≧3 AE that is considered to be possibly, probably, or definitely related to the study drug, with the following exceptions: (1) for nausea, emesis, diarrhea, rash, or mucositis, only Grade≧3 AE that do not respond within 48 hours to standard supportive/pharmacological treatment will be considered DLT; (2) for electrolyte imbalances, only Grade≧3 AE that do not respond to correction within 24 hours will be considered DLT. In addition, specific hematologic DLTs are defined as:

-   (i) Thrombocytopenia—Grade 4 of any duration, Grade 3 for ≧7 days,     or Grade 3 associated with clinically significant bleeding; -   (ii) Neutropenia—Grade 4 for ≧3 days, or any Grade≧3 febrile     neutropenia

The above criteria can be used to make individual patient determinations regarding dose reductions, interruptions or discontinuation throughout the course of the trial, but DLTs occurring during Cycle 1 will be used to inform safety and tolerability assessments for dose escalation decisions.

The “Maximum Tolerated Dose” (MTD) as used herein is defined as the dose at which ≦1 of 6 patients experiences a treatment-related toxicity that qualifies as a DLT, with the next higher dose having ≧2 of up to 6 patients experiencing a DLT. The MTD may not be established until all patients enrolled in the cohort have completed Cycle 1, discontinued treatment or had a dose reduction. Previously established tolerability of a dose level will be reevaluated if DLTs are observed in later cycles.

“Measurable disease” (MD) as used herein is defined by the presence of at least one measurable lesion.

Measurable lesions are defined as those that can be accurately measured in at least one dimension [longest diameter (LD) in the plane of measurement to be recorded] with a minimum size of: 10 mm by CT scan (CT scan slice thickness no greater than 5 mm), 10 mm caliper measurement by clinical exam (lesions which cannot be accurately measured with calipers can be recorded as non-measurable), or 20 mm by chest x-ray.

“Malignant lymph nodes” is to be considered pathologically enlarged and measurable if the lymph node is ≧15 mm in short axis when assessed by CT scan (CT scan slice thickness no greater than 5 mm)

“Non-measurable Disease” as used herein include all other lesions (or sites of disease) that are not measurable, including small lesions (longest diameter <10 mm or pathological lymph nodes with ≧10 to <15 mm short axis) are considered non-measurable disease. Lesions considered truly non-measurable include: leptomeningeal disease, ascites, pleural/pericardial effusions, lymphangitis cutis/pulmonis, inflammatory breast disease, abdominal masses/abdominal organomegaly identified by physical exam and not followed by CT or MRI.

“Target lesions” as used herein include all measurable lesions up to a maximum of two lesions per organ and five lesions in total, representative of all involved organs identified as target lesions and recorded and measured at baseline. Target lesions can be selected on the basis of their size (lesions with the longest diameter) and their suitability for accurate repeated measurements (either by imaging techniques or clinically). A sum of the diameters (longest for non-nodal lesions, short axis for nodal lesions) for all target lesions can be calculated and reported as the baseline sum diameters. The baseline sum diameters can be used as reference by which to characterize the objective tumor response.

“Non-target lesions” as used herein include all other lesions (or sites of disease) including pathological lymph nodes that are not target lesions. Non-target lesions can be identified as non-target lesions and can also be recorded at baseline. Measurements of these lesions may not be required and these lesions can be followed as “present,” “absent,” or in rare cases “unequivocal progression.” In addition, it can be possible to record multiple non-target lesions involving the same organ as a single item on the case report form (e.g., ‘multiple enlarged pelvic lymph nodes’ or ‘multiple liver metastases’).

“Complete response” (CR) as used herein is defined as the disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) must have reduction in short axis to <10 mm.

“Partial response (PR)” as used herein is defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters.

“Progressive disease (PD)” as used herein is defined as at least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest). In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of at least 5 mm. The appearance of one or more new lesions can also be considered progression.

“Stable disease” (SD) as used herein is defined as neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, taking as reference the smallest sum diameters while on study.

The term “subject” or “patient” encompasses mammals and non-mammals. Examples of mammals include, but are not limited to, humans; non-human primates such as chimpanzees, and other apes and monkey species; farm animals such as cattle, horses, sheep, goats, swine; domestic animals such as rabbits, dogs, and cats; laboratory animals including rodents, such as rats, mice and guinea pigs, and the like. Examples of non-mammals include, but are not limited to, birds, fish and the like. In one embodiment of the methods and compositions provided herein, the mammal is a human.

The term “haploinsufficient” means a condition that occurs when a diploid organism has only a single functional copy of a gene (with the other copy inactivated by mutation) and the single functional copy does not produce enough of a gene product (typically a protein) to bring about a wild-type condition, leading to an abnormal or diseased state.

The term “silent mutation” as used herein silent mutation is a type of mutation in the coding region of a gene that doesn't actually change the amino acid sequence of the protein that is made.

The details of one or more particular embodiments of the invention are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.

Overview

In one aspect, the disclosure provides a method of treating solid tumor in a subject. For example, the methods disclosed herein can be used for treating solid tumors that are not p53 negative. In some cases the methods disclosed herein can be used for treating solid tumor which has been determined to lack a p53 deactivating mutation. The methods of the disclosure can also be used to treat solid tumors that express gain of function mutant p53 i.e. a super apoptotic p53. In other examples, the methods of the disclosure are useful in treating solid tumors, wherein the solid tumor expresses p53 with a partial loss of function mutation, p53 with a copy loss mutation, or p53 with one or more silent mutations. In some example, the solid tumor expresses p53 with a copy loss mutation and a deactivating mutation.

The method comprises administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins. In some embodiments, the peptidomimetic macrocycle disrupts the interaction between p53 and MDM2 and MDMX.

In another aspect, the disclosure provides a method of treating solid tumor in a subject expressing wild type p53. The method comprises administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins. In some embodiments, the peptidomimetic macrocycle disrupts the interaction between p53 and MDM2 and MDMX.

In some embodiments the subject treated by the methods disclosed herein is a human. In some embodiments, a subject treated in accordance with the methods provided herein is a human who has or is diagnosed with solid tumor lacking p53 deactivating mutation and/or expressing wild type p53. In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human predisposed or susceptible to solid tumor lacking p53 deactivating mutation and/or expressing wild type p53. In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human at risk of developing solid tumor lacking p53 deactivating mutation and/or expressing wild type p53. A p53 deactivating mutation in some examples can be a mutation in DNA-binding domain of the p53 protein. In some examples the p53 deactivating mutation can be a missense mutation. In various examples, the solid tumor can be determined to lack one or more p53 deactivating mutations selected from mutations at one or more of residues R175, G245, R248, R249, R273, and R282. The lack of p53 deactivating mutation and/or the presence of wild type p53 in the solid tumor can be determined by any suitable method known in art, for example by sequencing, array based testing, RNA analysis and amplifications methods like PCR.

In certain embodiments, the human subject is refractory and/or intolerant to one or more other standard treatment of the solid tumor known in art. In some embodiments, the human subject has had at least one unsuccessful prior treatment and/or therapy of the solid tumor.

In some embodiments, the subject treated in accordance with the methods of the disclosure is a human who has or is diagnosed with solid tumor that is not p53 negative. In some embodiments, the subject treated in accordance with the methods of the disclosure is a human who has or is diagnosed with solid tumor that express gain of function mutant p53 i.e. a super apoptotic p53. In some embodiments, the subject treated in accordance with the methods of the disclosure is a human who has or is diagnosed with solid tumor that expresses p53 with a partial loss of function mutation. In some embodiments, the subject treated in accordance with the methods provided herein is a human who has or is diagnosed with solid tumor that expresses p53 with a copy loss mutation. In some embodiments, the subject treated in accordance with the methods provided herein is a human who has or is diagnosed with solid tumor that expresses p53 with one or more silent mutations. In some embodiments, the subject treated in accordance with the methods provided herein is a human who has or is diagnosed with solid tumor that expresses p53 with a copy loss mutation and a deactivating mutation.

In some embodiments, the methods for treating solid tumor provided herein inhibit, reduce, diminish, arrest, or stabilize a tumor associated with the solid tumor. In some embodiments, the methods for treating solid tumor provided herein inhibit, reduce, diminish, arrest, or stabilize the blood flow, metabolism, or edema in a tumor associated with the solid tumor or one or more symptoms thereof. In some embodiments, the methods for treating solid tumor provided herein cause the regression of a tumor, tumor blood flow, tumor metabolism, or peritumor edema, and/or one or more symptoms associated with the solid tumor. In some embodiments, the methods for treating solid tumor provided herein maintain the size of the tumor so that it does not increase, or so that it increases by less than the increase of a tumor after administration of a standard therapy as measured by conventional methods available to one of skill in the art, such as ultrasound, CT Scan, MRI, dynamic contrast-enhanced MRI, or PET Scan. In specific embodiments, the methods for treating solid tumor provided herein decrease tumor size. In some embodiments, the methods for treating solid tumor provided herein reduce the formation of a tumor. In certain embodiments, the methods for treating solid tumor provided herein eradicate, remove, or control primary, regional and/or metastatic tumors associated with the solid tumor. In some embodiments, the methods for treating solid tumor provided herein decrease the number or size of metastases associated with the solid tumor. In some embodiments, the methods for treating solid tumor provided herein result in complete response to the treatment. In some embodiments, the methods for treating solid tumor provided herein result in partial response to the treatment. In some embodiments, the solid tumor treated by the methods disclosed herein is a stable disease. In some embodiments, the solid tumor treated by the methods disclosed herein is a progressive disease.

Solid tumor cancers that can be treated by the methods provided herein include, but are not limited to, sarcomas, carcinomas, and lymphomas. In specific embodiments, solid tumors that can be treated in accordance with the methods described include, but are not limited to, cancer of the breast, liver, neuroblastoma, head, neck, eye, mouth, throat, esophagus, esophagus, chest, bone, lung, kidney, colon, rectum or other gastrointestinal tract organs, stomach, spleen, skeletal muscle, subcutaneous tissue, prostate, breast, ovaries, testicles or other reproductive organs, skin, thyroid, blood, lymph nodes, kidney, liver, pancreas, and brain or central nervous system.

The peptidomimetic macrocycle can be any cross-linked peptide, i.e. any peptide that comprises at least one macrocycle-forming linker which forms a macrocycle between a first amino acid residue (or analog) and a second amino acid residue. For example, the peptidomimetic macrocycle can be a peptidomimetic macrocycle capable of binding to the MDM2 and/or MDMX proteins. In some embodiments, the peptidomimetic macrocycles can be a peptidomimetic macrocycle of Formula I:

wherein: each of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ is individually an amino acid, wherein at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8) or Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9), where each X is an amino acid; each D and E is independently an amino acid; each R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or at least one of R₁ and R₂ forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids; each L or L′ is independently a macrocycle-forming each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₇ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue; each R₈ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue; each v is an integer from 1-1000, for example 1-500, 1-200, 1-100, 1-50, 1-30, 1-20, or 1-10; and each w is an integer from 0-1000, for example 1-500, 1-200, 1-100, 1-50, 1-30, 1-20, or 1-10.

Administration of the a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof can be achieved by any suitable means. For example the pharmaceutical composition can be administered parenterally. For example, administration can be intravenous, intra-arterial, intraosseous infusion, intra-muscular, intracerebral, intracerebroventricular, intrathecal, or subcutaneous. In some embodiments administration is performed intravenously.

In some embodiments, the methods disclosed herein additionally or optionally comprise evaluating the safety and/or tolerability of a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, of the disclosure in subjects with solid tumors determined to lack a p53 deactivating mutation or with solid tumors expressing wild-type (WT) p53 protein.

Also provided here in are methods to determine the dose limiting toxicities (DLT) and the maximum tolerated dose (MTD) of the peptidomimetic macrocycles disclosed herein in subjects with solid tumors determined to lack a p53 deactivating mutation or with solid tumors expressing wild-type (WT) p53 protein.

In some embodiments, the methods disclosed herein additionally or optionally comprise the pharmacokinetic (PK) analysis of the peptidomimetic macrocycles and/or its metabolites in blood following single and/or multiple administration of the peptidomimetic macrocycles to the subject.

In some embodiments, the methods disclosed herein additionally or optionally comprise studying the effect of the peptidomimetic macrocycles on pharmacodynamic biomarkers in tumor biopsy samples (e.g., p21, caspase, MDM2) and blood samples (e.g., macrophage inhibitory cytokine-1 [MIC-1]), and assessing possible correlation between these biomarkers and clinical response.

In some embodiments, the methods disclosed herein additionally or optionally include steps to assess potential patient biomarkers (e.g., p53 status, MDM2 and MDMX expression levels), the effect of the peptidomimetic macrocycles treatment on these biomarkers, and possible correlation between these biomarkers and clinical response of the peptidomimetic macrocycles.

Also provided herein are methods to evaluate clinical activity of the peptidomimetic macrocycles in subjects with specific tumor types lacking a p53 deactivating mutation and/or expressing WT p53 in the dose expansion phase.

Compound and Compositions Peptidomimetic Macrocycles

In some embodiments, a peptidomimetic macrocycle has the Formula (I):

wherein: each A, C, and D is independently an amino acid; each B is independently an amino acid,

[—NH-L₃-CO—], [—NH-L₃-SO₂—], or [—NH-L₃-]; each E is independently an amino acid selected from the group consisting of Ala (alanine), D-Ala (D-alanine), Aib (α-aminoisobutyric acid), Sar (N-methyl glycine), and Ser (serine); each R₃ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅; each R₁ and R₂ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids; each L and L′ is independently a macrocycle-forming linker; each L₃ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄—K—R₄-]_(n), each being optionally substituted with R₅; each R₄ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene; each K is independently O, S, SO, SO₂, CO, CO₂, or CONR₃; each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR_(E), —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₇ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue; each R₈ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue; each v is independently an integer; each w is independently an integer from 3-1000; u is an integer from 1-10; each x, y and z is independently an integer from 0-10; and each n is independently an integer from 1-5.

In some embodiments, each v and w is independently integers between 1-30. In some embodiments, w is an integer from 3-1000, for example 3-500, 3-200, 3-100, 3-50, 3-30, 3-20, or 3-10. In some embodiments, the sum of x+y+z is 3 or 6. In some embodiments, the sum of x+y+z is 3. In other embodiments, the sum of x+y+z is 6.

In some embodiments, peptidomimetic macrocycles are also provided of the formula:

wherein: each of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ is individually an amino acid, wherein at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8), where each X is an amino acid; each D and E is independently an amino acid; each R₁ and R₂ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or at least one of R₁ and R₂ forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids; each L or L′ is independently a macrocycle-forming linker; each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₇ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue; each R₈ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue; v is an integer from 1-1000, for example 1-500, 1-200, 1-100, 1-50, 1-30, 1-20 or 1-10; and w is an integer from 3-1000, for example 3-500, 3-200, 3-100, 3-50, 3-30, 3-20, or 3-10.

In some embodiments, each v and w is independently an integer between 1-30. In some embodiments, w is an integer from 3-1000, for example 3-500, 3-200, 3-100, 3-50, 3-30, 3-20, or 3-10. In some embodiments, the sum of x+y+z is 3 or 6. In some embodiments, the sum of x+y+z is 3. In other embodiments, the sum of x+y+z is 6.

In some embodiments of any of the Formulas described herein, at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₅, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8). In other embodiments, at least four of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8). In other embodiments, at least five of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8). In other embodiments, at least six of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8). In other embodiments, at least seven of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8).

In some embodiments, a peptidomimetic macrocycle has the Formula:

wherein: each of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ is individually an amino acid, wherein at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9), where each X is an amino acid; each D is independently an amino acid; each E is independently an amino acid, for example an amino acid selected from Ala (alanine), D-Ala (D-alanine), Aib (α-aminoisobutyric acid), Sar (N-methyl glycine), and Ser (serine); each R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or at least one of R₁ and R₂ forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids; each L or L′ is independently a macrocycle-forming linker; each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR_(E), —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₇ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue; each R₈ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue; v is an integer from 1-1000, for example 1-500, 1-200, 1-100, 1-50, 1-30, 1-20, or 1-10; w is an integer from 3-1000, for example 3-500, 3-200, 3-100, 3-50, 3-30, 3-20, or 3-10; and.

In some embodiments of the above Formula, at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9) In other embodiments of the above Formula, at least four of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9) In other embodiments of the above Formula, at least five of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9). In other embodiments of the above Formula, at least six of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₅-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9) In other embodiments of the above Formula, at least seven of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9).

In some embodiments, w is an integer from 3-10, for example 3-6, 3-8, 6-8, or 6-10. In some embodiments, w is 3. In other embodiments, w is 6. In some embodiments, v is an integer from 1-10, for example 2-5. In some embodiments, v is 2.

In some embodiments, a peptidomimetic macrocycle of Formula (I) has Formula (Ic):

wherein: each A, C, D, and E is independently a natural or non-natural amino acid; each B is independently a natural or non-natural amino acid, amino acid analog,

[—NH-L₃-CO—], [—NH-L₃-SO₂—], or [—NH-L₃-]; each L is independently a macrocycle-forming linker; each L′ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene, each being optionally substituted with R₅, or a bond, or together with R₁ and the atom to which both R₁ and L′ are bound forms a ring; each L″ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene, each being optionally substituted with R₅, or a bond, or together with R₂ and the atom to which both R₂ and L″ are bound forms a ring; each R₁ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-, or together with L′ and the atom to which both R₁ and L′ are bound forms a ring; each R₂ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-, or together with L″ and the atom to which both R₂ and L″ are bound forms a ring; R₃ is hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, aryl, or heteroaryl, optionally substituted with R₅; each L₃ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, heteroarylene, or [—R₄—K—R₄—]_(n), each being optionally substituted with R₅; each R₄ is alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene; each K is O, S, SO, SO₂, CO, CO₂, or CONR₃; each n is an integer from 1-5; each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR_(E), —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₇ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, aryl, or heteroaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue; each R₈ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, aryl, or heteroaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue; each v and w is independently an integer from 1-1000, for example 1-500, 1-200, 1-100, 1-50, 1-40, 1-25, 1-20, 1-15, or 1-10; and each u, x, y and z is independently an integer from 0-10.

In some embodiments, the peptidomimetic macrocycles have the Formula (I):

wherein: each A, C, D, and E is independently a natural or non-natural amino acid; each B is independently a natural or non-natural amino acid, amino acid analog,

[—NH-L₃-CO—], [—NH-L₃-SO₂—], or [—NH-L₃-]; each R₁ and R₂ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; each R₃ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, aryl, or heteroaryl, optionally substituted with R₅; each L is independently a macrocycle-forming linker of the formula

each L₁, L₂ and L₃ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, heteroarylene, or [—R₄—K—R₄—]_(n), each being optionally substituted with R₅; each R₄ is alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene; each K is independently O, S, SO, SO₂, CO, CO₂, or CONR₃; each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR_(E), —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₇ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, aryl, or heteroaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue; each R₈ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, aryl, or heteroaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue; each v and w is independently an integer from 1-1000; each u, x, y and z is independently integers from 0-10; and n is an integer from 1-5.

In an embodiment of any of the Formulas described herein, of the macrocycle-forming linker (L) has a formula -L₁-L₂-, wherein

each L₁ and L₂ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄—K—R₄—]_(n), each being optionally substituted with R₅; each R₄ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene; each K is independently O, S, SO, SO₂, CO, CO₂, or CONR₃; each R₃ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅; and n is an integer from 1-5.

In some embodiments in the Formulas described herein, L (or L′) is a macrocycle-forming linker of the formula

Exemplary embodiments of such macrocycle-forming linkers L are shown below.

In an embodiment of any of the Formulas described herein, L₁ and L₂, either alone or in combination, form a triazole or a thioether.

In an embodiment of any of the Formulas described herein, L₁ and L₂, either alone or in combination, do not form a triazole or a thioether.

In one example, at least one of R₁ and R₂ is alkyl, unsubstituted or substituted with halo-. In another example, each R₁ and R₂ are independently alkyl, unsubstituted or substituted with halo-. In some embodiments, at least one of R₁ and R₂ is methyl. In other embodiments, R₁ and R₂ are methyl.

In some embodiments, x+y+z is at least 3. In other embodiments, x+y+z is 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10. In some embodiments, the sum of x+y+z is 3 or 6. In some embodiments, the sum of x+y+z is 3. In other embodiments, the sum of x+y+z is 6. Each occurrence of A, B, C, D or E in a macrocycle or macrocycle precursor is independently selected. For example, a sequence represented by the formula [A]_(x), when x is 3, encompasses embodiments where the amino acids are not identical, e.g. Gln-Asp-Ala as well as embodiments where the amino acids are identical, e.g. Gln-Gln-Gln. This applies for any value of x, y, or z in the indicated ranges. Similarly, when u is greater than 1, each compound can encompass peptidomimetic macrocycles which are the same or different. For example, a compound can comprise peptidomimetic macrocycles comprising different linker lengths or chemical compositions.

In some embodiments, the peptidomimetic macrocycle comprises a secondary structure which is an α-helix and R₈ is —H, allowing intrahelical hydrogen bonding. In some embodiments, at least one of A, B, C, D or E is an α,α-disubstituted amino acid. In one example, B is an α,α-disubstituted amino acid. For instance, at least one of A, B, C, D or E is 2-aminoisobutyric acid. In other embodiments, at least one of A, B, C, D or E is

In other embodiments, the length of the macrocycle-forming linker L as measured from a first Cα to a second Cα is selected to stabilize a desired secondary peptide structure, such as an α-helix formed by residues of the peptidomimetic macrocycle including, but not necessarily limited to, those between the first Cα to a second Cα.

In one embodiment, the peptidomimetic macrocycle of Formula (I) is:

wherein each R₁ and R₂ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-.

In related embodiments, the peptidomimetic macrocycle of Formula (I) is:

wherein each R₁′ and R₂′ is independently an amino acid.

In other embodiments, the peptidomimetic macrocycle of Formula (I) is a compound of any of the formulas shown below:

wherein “AA” represents any natural or non-natural amino acid side chain and ‘

’ is [D]_(v), [E]_(w) as defined above, and n is an integer between 0 and 20, 50, 100, 200, 300, 400 or 500. In some embodiments, n is 0. In other embodiments, n is less than 50.

Exemplary embodiments of the macrocycle-forming linker L are shown below.

In other embodiments, D and/or E in the compound of Formula I are further modified in order to facilitate cellular uptake. In some embodiments, lipidating or PEGylating a peptidomimetic macrocycle facilitates cellular uptake, increases bioavailability, increases blood circulation, alters pharmacokinetics, decreases immunogenicity and/or decreases the needed frequency of administration.

In other embodiments, at least one of [D] and [E] in the compound of Formula I represents a moiety comprising an additional macrocycle-forming linker such that the peptidomimetic macrocycle comprises at least two macrocycle-forming linkers. In a specific embodiment, a peptidomimetic macrocycle comprises two macrocycle-forming linkers. In an embodiment, u is 2.

In some embodiments, any of the macrocycle-forming linkers described herein can be used in any combination with any of the sequences shown in Table 3, Table 3a, Table 3b, or Table 3c and also with any of the R-substituents indicated herein.

In some embodiments, the peptidomimetic macrocycle comprises at least one α-helix motif. For example, A, B and/or C in the compound of Formula I include one or more α-helices. As a general matter, α-helices include between 3 and 4 amino acid residues per turn. In some embodiments, the α-helix of the peptidomimetic macrocycle includes 1 to 5 turns and, therefore, 3 to 20 amino acid residues. In specific embodiments, the α-helix includes 1 turn, 2 turns, 3 turns, 4 turns, or 5 turns. In some embodiments, the macrocycle-forming linker stabilizes an α-helix motif included within the peptidomimetic macrocycle. Thus, in some embodiments, the length of the macrocycle-forming linker L from a first Cα to a second Cα is selected to increase the stability of an α-helix. In some embodiments, the macrocycle-forming linker spans from 1 turn to 5 turns of the α-helix. In some embodiments, the macrocycle-forming linker spans approximately 1 turn, 2 turns, 3 turns, 4 turns, or 5 turns of the α-helix. In some embodiments, the length of the macrocycle-forming linker is approximately 5 Å to 9 Å per turn of the α-helix, or approximately 6 Å to 8 Å per turn of the α-helix. Where the macrocycle-forming linker spans approximately 1 turn of an α-helix, the length is equal to approximately 5 carbon-carbon bonds to 13 carbon-carbon bonds, approximately 7 carbon-carbon bonds to 11 carbon-carbon bonds, or approximately 9 carbon-carbon bonds. Where the macrocycle-forming linker spans approximately 2 turns of an α-helix, the length is equal to approximately 8 carbon-carbon bonds to 16 carbon-carbon bonds, approximately 10 carbon-carbon bonds to 14 carbon-carbon bonds, or approximately 12 carbon-carbon bonds. Where the macrocycle-forming linker spans approximately 3 turns of an α-helix, the length is equal to approximately 14 carbon-carbon bonds to 22 carbon-carbon bonds, approximately 16 carbon-carbon bonds to 20 carbon-carbon bonds, or approximately 18 carbon-carbon bonds. Where the macrocycle-forming linker spans approximately 4 turns of an α-helix, the length is equal to approximately 20 carbon-carbon bonds to 28 carbon-carbon bonds, approximately 22 carbon-carbon bonds to 26 carbon-carbon bonds, or approximately 24 carbon-carbon bonds. Where the macrocycle-forming linker spans approximately 5 turns of an α-helix, the length is equal to approximately 26 carbon-carbon bonds to 34 carbon-carbon bonds, approximately 28 carbon-carbon bonds to 32 carbon-carbon bonds, or approximately 30 carbon-carbon bonds. Where the macrocycle-forming linker spans approximately 1 turn of an α-helix, the linkage contains approximately 4 atoms to 12 atoms, approximately 6 atoms to 10 atoms, or approximately 8 atoms. Where the macrocycle-forming linker spans approximately 2 turns of the α-helix, the linkage contains approximately 7 atoms to 15 atoms, approximately 9 atoms to 13 atoms, or approximately 11 atoms. Where the macrocycle-forming linker spans approximately 3 turns of the α-helix, the linkage contains approximately 13 atoms to 21 atoms, approximately 15 atoms to 19 atoms, or approximately 17 atoms. Where the macrocycle-forming linker spans approximately 4 turns of the α-helix, the linkage contains approximately 19 atoms to 27 atoms, approximately 21 atoms to 25 atoms, or approximately 23 atoms. Where the macrocycle-forming linker spans approximately 5 turns of the α-helix, the linkage contains approximately 25 atoms to 33 atoms, approximately 27 atoms to 31 atoms, or approximately 29 atoms. Where the macrocycle-forming linker spans approximately 1 turn of the α-helix, the resulting macrocycle forms a ring containing approximately 17 members to 25 members, approximately 19 members to 23 members, or approximately 21 members. Where the macrocycle-forming linker spans approximately 2 turns of the α-helix, the resulting macrocycle forms a ring containing approximately 29 members to 37 members, approximately 31 members to 35 members, or approximately 33 members. Where the macrocycle-forming linker spans approximately 3 turns of the α-helix, the resulting macrocycle forms a ring containing approximately 44 members to 52 members, approximately 46 members to 50 members, or approximately 48 members. Where the macrocycle-forming linker spans approximately 4 turns of the α-helix, the resulting macrocycle forms a ring containing approximately 59 members to 67 members, approximately 61 members to 65 members, or approximately 63 members. Where the macrocycle-forming linker spans approximately 5 turns of the α-helix, the resulting macrocycle forms a ring containing approximately 74 members to 82 members, approximately 76 members to 80 members, or approximately 78 members.

In other embodiments, provided are peptidomimetic macrocycles of Formula (IV) or (IVa):

wherein: each A, C, D, and E is independently a natural or non-natural amino acid, and the terminal D and E independently optionally include a capping group; each B is a natural or non-natural amino acid, amino acid analog,

[—NH-L₃-CO—], [—NH-L₃-SO₂—], or [—NH-L₃-];

each R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or at least one of R₁ and R₂ forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids;

each R₃ is hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅; each L is a macrocycle-forming linker of the formula -L₁-L₂-; each L₁, L₂ and L₃ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄—K—R₄—]_(n), each being optionally substituted with R₅; each R₄ is alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene; each K is O, S, SO, SO₂, CO, CO₂, or CONR₃; each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR_(E), —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₇ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅; each v and w are independently integers from 1-1000; u is an integer from 1-10; each x, y and z are independently integers from 0-10; and each n is an integer from 1-5.

In one example, L₁ and L₂, either alone or in combination, do not form a triazole or a thioether.

In one example, at least one of R₁ and R₂ is alkyl, unsubstituted or substituted with halo-. In another example, both R₁ and R₂ are independently alkyl, unsubstituted or substituted with halo-. In some embodiments, at least one of R₁ and R₂ is methyl. In other embodiments, R₁ and R₂ are methyl.

In some embodiments, x+y+z is at least 1. In other embodiments, x+y+z is at least 2. In other embodiments, x+y+z is 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10. Each occurrence of A, B, C, D or E in a macrocycle or macrocycle precursor is independently selected. For example, a sequence represented by the formula [A]_(x), when x is 3, encompasses embodiments where the amino acids are not identical, e.g. Gln-Asp-Ala as well as embodiments where the amino acids are identical, e.g. Gln-Gln-Gln. This applies for any value of x, y, or z in the indicated ranges.

In some embodiments, the peptidomimetic macrocycle comprises a secondary structure which is an α-helix and R₈ is —H, allowing intrahelical hydrogen bonding. In some embodiments, at least one of A, B, C, D or E is an α,α-disubstituted amino acid. In one example, B is an α,α-disubstituted amino acid. For instance, at least one of A, B, C, D or E is 2-aminoisobutyric acid. In other embodiments, at least one of A, B, C, D or E is

In other embodiments, the length of the macrocycle-forming linker L as measured from a first Cα to a second Cα is selected to stabilize a desired secondary peptide structure, such as an α-helix formed by residues of the peptidomimetic macrocycle including, but not necessarily limited to, those between the first Cα to a second Cα.

Exemplary embodiments of the macrocycle-forming linker -L₁-L₂-are shown below.

Unless otherwise stated, any compounds (including peptidomimetic macrocycles, macrocycle precursors, and other compositions) are also meant to encompass compounds which differ only in the presence of one or more isotopically enriched atoms. For example, compounds having the described structures except for the replacement of a hydrogen by a deuterium or tritium, or the replacement of a carbon by ¹³C- or ¹⁴C-enriched carbon are within the scope of this disclosure.

In some embodiments, the compounds disclosed herein can contain unnatural proportions of atomic isotopes at one or more of atoms that constitute such compounds. For example, the compounds can be radiolabeled with radioactive isotopes, such as for example tritium (³H), iodine-125 (¹²⁵I) or carbon-14 (¹⁴C). In other embodiments, one or more carbon atoms is replaced with a silicon atom. All isotopic variations of the compounds disclosed herein, whether radioactive or not, are contemplated herein.

The circulating half-life of the peptidomimetic macrocycles in human blood can be about 1-24 h. For example the circulating half-life of the peptidomimetic macrocycles in human blood can be about 2-24 h, 4-24 h, 6-24 h, 8-24 h, 10-24 h, 12-24 h, 14-24 h, 16-24 h, 18-24 h, 20-24 h, 22-24 h, 1-20 h, 4-20 h, 6-20 h, 8-20 h, 10-20 h, 12-20 h, 14-20 h, 16-20 h, 18-20 h, 1-16 h, 4-16 h, 6-16 h, 8-16 h, 10-16 h, 12-16 h, 14-16 h, 1-12 h, 4-12 h, 6-12 h, 8-12 h, 10-12 h, 1-8 h, 4-8 h, 6-8 h, or 1-4 h. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood can be bout 1-12 h, for example about 1 h, 2 h, 3 h, 4 h, 5 h, 6 h, 7 h, 8 h, 9 h, 10 h, 11 h, or 12 h. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood is about 2 h. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood is about 4 h. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood is about 6 h. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood is about 8 h. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood is about 10 h.

The half-life of the peptidomimetic macrocycles in biological tissue can be about 1-24 h. For example the circulating half-life of the peptidomimetic macrocycles in human blood can be about 1-24 h, 5-24 h, 10-24 h, 15-24 h, 20-24 h, 1-22 h, 5-22 h, 10-22 h, 15-22 h, 20-22 h, 1-20 h, 5-20 h, 15-20 h, 1-18 h, 5-18 h, 10-18 h, 15-18 h, 1-16 h, 5-16 h, 10-16 h, 15-16 h, 1-14 h, 5-14 h, 10-14 h, 1-12 h, 5-12 h, 10-12 h, 1-10 h, 5-10 h, 1-8 h, 5-8 h, 1-6 h, 5-6 h, or 1-4 h. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood can be bout 5-20 h, for example about 5 h, 6 h, 7 h, 8 h, 9 h, 10 h, 11 h, 12 h, 13 h, 14 h, 15 h, 16 h, 17 h, 18 h, 19 h or 20 h. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood is about 2 h. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood is about 4 h. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood is about 6 h. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood is about 8 h. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood is about 10 h.

The circulating half-life of the peptidomimetic macrocycles in human blood can be greater than, equal to, or less than the half-life of the peptidomimetic macrocycles in biological tissue. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood can be greater than the half-life of the peptidomimetic macrocycles in biological tissue. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood can be equal to the half-life of the peptidomimetic macrocycles in biological tissue. In some examples, the half-life of the peptidomimetic macrocycles in biological tissue is greater than the circulating half-life of the peptidomimetic macrocycles in human blood. This can facilitate administration of the peptidomimetic macrocycles at a lower dose and/or at lower frequency. In some embodiments, the half-life of the peptidomimetic macrocycles in biological tissue is at least 1 h, 2 h, 3 h, 4 h, 5 h, 6 h, 7 h, 8 h, 9 h, 10 h, 11 h, or 12 h greater than the than the circulating half-life of the peptidomimetic macrocycles in human blood. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood is about 4 h and the half-life of the in biological tissue is about 10 h. In some examples, the circulating half-life of the peptidomimetic macrocycles in human blood is about 6 h and the half-life of the in biological tissue is about 10 h.

Preparation of Peptidomimetic Macrocycles

Peptidomimetic macrocycles can be prepared by any of a variety of methods known in the art. For example, any of the residues indicated by “$” or “$r8” in Table 3, Table 3a, Table 3b, or Table 3c can be substituted with a residue capable of forming a crosslinker with a second residue in the same molecule or a precursor of such a residue.

Various methods to effect formation of peptidomimetic macrocycles are known in the art. For example, the preparation of peptidomimetic macrocycles of Formula I is described in Schafmeister et al., J. Am. Chem. Soc. 122:5891-5892 (2000); Schafmeister & Verdine, J. Am. Chem. Soc. 122:5891 (2005); Walensky et al., Science 305:1466-1470 (2004); U.S. Pat. No. 7,192,713 and PCT application WO 2008/121767. The α,α-disubstituted amino acids and amino acid precursors disclosed in the cited references can be employed in synthesis of the peptidomimetic macrocycle precursor polypeptides. For example, the “55-olefin amino acid” is (S)-α-(2′-pentenyl) alanine and the “R8 olefin amino acid” is (R)-α-(2′-octenyl) alanine. Following incorporation of such amino acids into precursor polypeptides, the terminal olefins are reacted with a metathesis catalyst, leading to the formation of the peptidomimetic macrocycle. In various embodiments, the following amino acids can be employed in the synthesis of the peptidomimetic macrocycle:

In other embodiments, the peptidomimetic macrocycles are of Formula IV or IVa. Methods for the preparation of such macrocycles are described, for example, in U.S. Pat. No. 7,202,332.

Additional methods of forming peptidomimetic macrocycles which are envisioned as suitable include those disclosed by Mustapa, M. Firouz Mohd et al., J. Org. Chem (2003), 68, pp. 8193-8198; Yang, Bin et al. Bioorg Med. Chem. Lett. (2004), 14, pp. 1403-1406; U.S. Pat. No. 5,364,851; U.S. Pat. No. 5,446,128; U.S. Pat. No. 5,824,483; U.S. Pat. No. 6,713,280; and U.S. Pat. No. 7,202,332. In such embodiments, amino acid precursors are used containing an additional substituent R— at the alpha position. Such amino acids are incorporated into the macrocycle precursor at the desired positions, which can be at the positions where the crosslinker is substituted or, alternatively, elsewhere in the sequence of the macrocycle precursor. Cyclization of the precursor is then effected according to the indicated method.

The peptidomimetic macrocycles described herein can be at least 1% pure, at least 2% pure, at least 3% pure, at least 4% pure, at least 5% pure, at least 6% pure, at least 7% pure, at least 8% pure, at least 9% pure, at least 10% pure, at least 11% pure, at least 12% pure, at least 13% pure, at least 14% pure, at least 15% pure, at least 16% pure, at least 17% pure, at least 18% pure, at least 19% pure, at least 20% pure, at least 21% pure, at least 22% pure, at least 23% pure, at least 24% pure, at least 25% pure, at least 26% pure, at least 27% pure, at least 28% pure, at least 29% pure, at least 30% pure, at least 31% pure, at least 32% pure, at least 33% pure, at least 34% pure, at least 35% pure, at least 36% pure, at least 37% pure, at least 38% pure, at least 39% pure, at least 40% pure, at least 41% pure, at least 42% pure, at least 43% pure, at least 44% pure, at least 45% pure, at least 46% pure, at least 47% pure, at least 48% pure, at least 49% pure, at least 50% pure, at least 51% pure, at least 52% pure, at least 53% pure, at least 54% pure, at least 55% pure, at least 56% pure, at least 57% pure, at least 58% pure, at least 59% pure, at least 60% pure, at least 61% pure, at least 62% pure, at least 63% pure, at least 64% pure, at least 65% pure, at least 66% pure, at least 67% pure, at least 68% pure, at least 69% pure, at least 70% pure, at least 71% pure, at least 72% pure, at least 73% pure, at least 74% pure, at least 75% pure, at least 76% pure, at least 77% pure, at least 78% pure, at least 79% pure, at least 80% pure, at least 81% pure, at least 82% pure, at least 83% pure, at least 84% pure, at least 85% pure, at least 86% pure, at least 87% pure, at least 88% pure, at least 89% pure, at least 90% pure, at least 91% pure, at least 92% pure, at least 93% pure, at least 94% pure, at least 95% pure, at least 96% pure, at least 97% pure, at least 98% pure, at least 99% pure, at least 99.1% pure, at least 99.2% pure, at least 99.3% pure, at least 99.4% pure, at least 99.5% pure, at least 99.6% pure, at least 99.7% pure, at least 99.8% pure, or at least 99.9% pure on a chemical, optical, isomeric, enantiomeric, or diastereomeric basis. Purity can be assessed, for example, by HPLC, MS, LC/MS, melting point, or NMR.

Two or more peptides/peptidomimetic macrocycles can share a degree of homology. A pair of peptides/peptidomimetic macrocycles can have, for example, up to about 20% pairwise homology, up to about 25% pairwise homology, up to about 30% pairwise homology, up to about 35% pairwise homology, up to about 40% pairwise homology, up to about 45% pairwise homology, up to about 50% pairwise homology, up to about 55% pairwise homology, up to about 60% pairwise homology, up to about 65% pairwise homology, up to about 70% pairwise homology, up to about 75% pairwise homology, up to about 80% pairwise homology, up to about 85% pairwise homology, up to about 90% pairwise homology, up to about 95% pairwise homology, up to about 96% pairwise homology, up to about 97% pairwise homology, up to about 98% pairwise homology, up to about 99% pairwise homology, up to about 99.5% pairwise homology, or up to about 99.9% pairwise homology. A pair of peptides can have, for example, at least about 20% pairwise homology, at least about 25% pairwise homology, at least about 30% pairwise homology, at least about 35% pairwise homology, at least about 40% pairwise homology, at least about 45% pairwise homology, at least about 50% pairwise homology, at least about 55% pairwise homology, at least about 60% pairwise homology, at least about 65% pairwise homology, at least about 70% pairwise homology, at least about 75% pairwise homology, at least about 80% pairwise homology, at least about 85% pairwise homology, at least about 90% pairwise homology, at least about 95% pairwise homology, at least about 96% pairwise homology, at least about 97% pairwise homology, at least about 98% pairwise homology, at least about 99% pairwise homology, at least about 99.5% pairwise homology, at least about 99.9% pairwise homology.

Various methods and software programs can be used to determine the homology between two or more peptides, such as NCBI BLAST, Clustal W, MAFFT, Clustal Omega, AlignMe, Praline, or another suitable method or algorithm.

Assays

The properties of peptidomimetic macrocycles are assayed, for example, by using the methods described below. In some embodiments, a peptidomimetic macrocycle has improved biological properties relative to a corresponding polypeptide lacking the substituents described herein.

Assay to Determine α-Helicity

In solution, the secondary structure of polypeptides with α-helical domains will reach a dynamic equilibrium between random coil structures and α-helical structures, often expressed as a “percent helicity”. Thus, for example, alpha-helical domains are predominantly random coils in solution, with α-helical content usually under 25%. Peptidomimetic macrocycles with optimized linkers, on the other hand, possess, for example, an alpha-helicity that is at least two-fold greater than that of a corresponding uncrosslinked polypeptide. In some embodiments, macrocycles will possess an alpha-helicity of greater than 50%. To assay the helicity of peptidomimetic macrocycles, the compounds are dissolved in an aqueous solution (e.g. 50 mM potassium phosphate solution at pH 7, or distilled H₂O, to concentrations of 25-50 μM). Circular dichroism (CD) spectra are obtained on a spectropolarimeter (e.g., Jasco J-710) using standard measurement parameters (e.g. temperature, 20° C.; wavelength, 190-260 nm; step resolution, 0.5 nm; speed, 20 nm/sec; accumulations, 10; response, 1 sec; bandwidth, 1 nm; path length, 0.1 cm). The α-helical content of each peptide is calculated by dividing the mean residue ellipticity (e.g. [Φ]222obs) by the reported value for a model helical decapeptide (Yang et al. (1986), Methods Enzymol. 130:208)).

Assay to Determine Melting Temperature (Tm)

A peptidomimetic macrocycle comprising a secondary structure such as an α-helix exhibits, for example, a higher melting temperature than a corresponding uncrosslinked polypeptide. Typically peptidomimetic macrocycles exhibit Tm of >60° C. representing a highly stable structure in aqueous solutions. To assay the effect of macrocycle formation on melting temperature, peptidomimetic macrocycles or unmodified peptides are dissolved in distilled H₂O (e.g. at a final concentration of 50 μM) and the Tm is determined by measuring the change in ellipticity over a temperature range (e.g. 4 to 95° C.) on a spectropolarimeter (e.g., Jasco J-710) using standard parameters (e.g. wavelength 222 nm; step resolution, 0.5 nm; speed, 20 nm/sec; accumulations, 10; response, 1 sec; bandwidth, 1 nm; temperature increase rate: 1° C./min; path length, 0.1 cm).

Protease Resistance Assay

The amide bond of the peptide backbone is susceptible to hydrolysis by proteases, thereby rendering peptidic compounds vulnerable to rapid degradation in vivo. Peptide helix formation, however, typically buries the amide backbone and therefore can shield it from proteolytic cleavage. The peptidomimetic macrocycles can be subjected to in vitro trypsin proteolysis to assess for any change in degradation rate compared to a corresponding uncrosslinked polypeptide. For example, the peptidomimetic macrocycle and a corresponding uncrosslinked polypeptide are incubated with trypsin agarose and the reactions quenched at various time points by centrifugation and subsequent HPLC injection to quantitate the residual substrate by ultraviolet absorption at 280 nm. Briefly, the peptidomimetic macrocycle and peptidomimetic precursor (5 mcg) are incubated with trypsin agarose (Pierce) (S/E˜125) for 0, 10, 20, 90, and 180 minutes. Reactions are quenched by tabletop centrifugation at high speed; remaining substrate in the isolated supernatant is quantified by HPLC-based peak detection at 280 nm. The proteolytic reaction displays first order kinetics and the rate constant, k, is determined from a plot of ln [S] versus time (k=−1Xslope).

Ex Vivo Stability Assay

Peptidomimetic macrocycles with optimized linkers possess, for example, an ex vivo half-life that is at least two-fold greater than that of a corresponding uncrosslinked polypeptide, and possess an ex vivo half-life of 12 hours or more. For ex vivo serum stability studies, a variety of assays can be used. For example, a peptidomimetic macrocycle and a corresponding uncrosslinked polypeptide (2 mcg) are incubated with fresh mouse, rat and/or human serum (2 mL) at 37° C. for 0, 1, 2, 4, 8, and 24 hours. To determine the level of intact compound, the following procedure can be used: The samples are extracted by transferring 100 μl of sera to 2 ml centrifuge tubes followed by the addition of 10 μL of 50% formic acid and 500 μL acetonitrile and centrifugation at 14,000 RPM for 10 min at 4±2° C. The supernatants are then transferred to fresh 2 ml tubes and evaporated on Turbovap under N₂<10 psi, 37° C. The samples are reconstituted in 100 μL of 50:50 acetonitrile:water and submitted to LC-MS/MS analysis.

In Vitro Binding Assays

To assess the binding and affinity of peptidomimetic macrocycles and peptidomimetic precursors to acceptor proteins, a fluorescence polarization assay (FPA) is used, for example. The FPA technique measures the molecular orientation and mobility using polarized light and fluorescent tracer. When excited with polarized light, fluorescent tracers (e.g., FITC) attached to molecules with high apparent molecular weights (e.g. FITC-labeled peptides bound to a large protein) emit higher levels of polarized fluorescence due to their slower rates of rotation as compared to fluorescent tracers attached to smaller molecules (e.g. FITC-labeled peptides that are free in solution).

For example, fluoresceinated peptidomimetic macrocycles (25 nM) are incubated with the acceptor protein (25-1000 nM) in binding buffer (140 mM NaCl, 50 mM Tris-HCL, pH 7.4) for 30 minutes at room temperature. Binding activity is measured, for example, by fluorescence polarization on a luminescence spectrophotometer (e.g. Perkin-Elmer LS50B). Kd values can be determined by nonlinear regression analysis using, for example, Graphpad Prism software (GraphPad Software, Inc., San Diego, Calif.). A peptidomimetic macrocycle shows, In some embodiments, similar or lower Kd than a corresponding uncrosslinked polypeptide.

In Vitro Displacement Assays to Characterize Antagonists of Peptide-Protein Interactions

To assess the binding and affinity of compounds that antagonize the interaction between a peptide and an acceptor protein, a fluorescence polarization assay (FPA) utilizing a fluoresceinated peptidomimetic macrocycle derived from a peptidomimetic precursor sequence is used, for example. The FPA technique measures the molecular orientation and mobility using polarized light and fluorescent tracer. When excited with polarized light, fluorescent tracers (e.g., FITC) attached to molecules with high apparent molecular weights (e.g. FITC-labeled peptides bound to a large protein) emit higher levels of polarized fluorescence due to their slower rates of rotation as compared to fluorescent tracers attached to smaller molecules (e.g. FITC-labeled peptides that are free in solution). A compound that antagonizes the interaction between the fluoresceinated peptidomimetic macrocycle and an acceptor protein will be detected in a competitive binding FPA experiment.

For example, putative antagonist compounds (1 nM to 1 mM) and a fluoresceinated peptidomimetic macrocycle (25 nM) are incubated with the acceptor protein (50 nM) in binding buffer (140 mM NaCl, 50 mM Tris-HCL, pH 7.4) for 30 minutes at room temperature. Antagonist binding activity is measured, for example, by fluorescence polarization on a luminescence spectrophotometer (e.g. Perkin-Elmer LS50B). Kd values can be determined by nonlinear regression analysis using, for example, Graphpad Prism software (GraphPad Software, Inc., San Diego, Calif.).

Any class of molecule, such as small organic molecules, peptides, oligonucleotides or proteins can be examined as putative antagonists in this assay.

Assay for Protein-Ligand Binding by Affinity Selection-Mass Spectrometry

To assess the binding and affinity of test compounds for proteins, an affinity-selection mass spectrometry assay is used, for example. Protein-ligand binding experiments are conducted according to the following representative procedure outlined for a system-wide control experiment using 1 μM peptidomimetic macrocycle plus 5 μM hMDM2. A 1 μL DMSO aliquot of a 40 μM stock solution of peptidomimetic macrocycle is dissolved in 19 μL of PBS (Phosphate-buffered saline: 50 mM, pH 7.5 Phosphate buffer containing 150 mM NaCl). The resulting solution is mixed by repeated pipetting and clarified by centrifugation at 10 000 g for 10 min. To a 4 μL aliquot of the resulting supernatant is added 4 μL of 10 μM hMDM2 in PBS. Each 8.0 μL experimental sample thus contains 40 pmol (1.5 μg) of protein at 5.0 μM concentration in PBS plus 1 μM peptidomimetic macrocycle and 2.5% DMSO. Duplicate samples thus prepared for each concentration point are incubated for 60 min at room temperature, and then chilled to 4° C. prior to size-exclusion chromatography-LC-MS analysis of 5.0 μL injections. Samples containing a target protein, protein-ligand complexes, and unbound compounds are injected onto an SEC column, where the complexes are separated from non-binding component by a rapid SEC step. The SEC column eluate is monitored using UV detectors to confirm that the early-eluting protein fraction, which elutes in the void volume of the SEC column, is well resolved from unbound components that are retained on the column. After the peak containing the protein and protein-ligand complexes elutes from the primary UV detector, it enters a sample loop where it is excised from the flow stream of the SEC stage and transferred directly to the LC-MS via a valving mechanism. The (M+3H)³⁺ ion of the peptidomimetic macrocycle is observed by ESI-MS at the expected m/z, confirming the detection of the protein-ligand complex.

Assay for Protein-Ligand Kd Titration Experiments

To assess the binding and affinity of test compounds for proteins, a protein-ligand Kd titration experiment is performed, for example. Protein-ligand K_(d) titrations experiments are conducted as follows: 2 μL DMSO aliquots of a serially diluted stock solution of titrant peptidomimetic macrocycle (5, 2.5, . . . , 0.098 mM) are prepared then dissolved in 38 μL of PBS. The resulting solutions are mixed by repeated pipetting and clarified by centrifugation at 10 000 g for 10 min. To 4.0 μL aliquots of the resulting supernatants is added 4.0 μL of 10 μM hMDM2 in PBS. Each 8.0 μL experimental sample thus contains 40 pmol (1.5 μg) of protein at 5.0 μM concentration in PBS, varying concentrations (125, 62.5, . . . , 0.24 μM) of the titrant peptide, and 2.5% DMSO. Duplicate samples thus prepared for each concentration point are incubated at room temperature for 30 min, then chilled to 4° C. prior to SEC-LC-MS analysis of 2.0 μL injections. The (M+H)¹⁺, (M+2H)²⁺, (M+3H)³⁺, and/or (M+Na)¹⁺ ion is observed by ESI-MS; extracted ion chromatograms are quantified, then fit to equations to derive the binding affinity K_(d) as described in “A General Technique to Rank Protein-Ligand Binding Affinities and Determine Allosteric vs. Direct Binding Site Competition in Compound Mixtures.” Annis, D. A.; Nazef, N.; Chuang, C. C.; Scott, M. P.; Nash, H. M. J. Am. Chem. Soc. 2004, 126, 15495-15503; also in “ALIS: An Affinity Selection-Mass Spectrometry System for the Discovery and Characterization of Protein-Ligand Interactions” D. A. Annis, C.-C. Chuang, and N. Nazef. In Mass Spectrometry in Medicinal Chemistry. Edited by Wanner K, Hofner G: Wiley-VCH; 2007:121-184. Mannhold R, Kubinyi H, Folkers G (Series Editors): Methods and Principles in Medicinal Chemistry.

Assay for Competitive Binding Experiments by Affinity Selection-Mass Spectrometry

To determine the ability of test compounds to bind competitively to proteins, an affinity selection mass spectrometry assay is performed, for example. A mixture of ligands at 40 μM per component is prepared by combining 2 μL aliquots of 400 μM stocks of each of the three compounds with 14 μL of DMSO. Then, 1 μL aliquots of this 40 μM per component mixture are combined with 1 μL DMSO aliquots of a serially diluted stock solution of titrant peptidomimetic macrocycle (10, 5, 2.5, . . . , 0.078 mM). These 2 μL samples are dissolved in 38 μL of PBS. The resulting solutions were mixed by repeated pipetting and clarified by centrifugation at 10 000 g for 10 min. To 4.0 μL aliquots of the resulting supernatants is added 4.0 μL of 10 μM hMDM2 protein in PBS. Each 8.0 μL experimental sample thus contains 40 pmol (1.5 μg) of protein at 5.0 μM concentration in PBS plus 0.5 μM ligand, 2.5% DMSO, and varying concentrations (125, 62.5, . . . , 0.98 μM) of the titrant peptidomimetic macrocycle. Duplicate samples thus prepared for each concentration point are incubated at room temperature for 60 min, then chilled to 4° C. prior to SEC-LC-MS analysis of 2.0 μL injections. Additional details on these and other methods are provided in “A General Technique to Rank Protein-Ligand Binding Affinities and Determine Allosteric vs. Direct Binding Site Competition in Compound Mixtures.” Annis, D. A.; Nazef, N.; Chuang, C. C.; Scott, M. P.; Nash, H. M. J. Am. Chem. Soc. 2004, 126, 15495-15503; also in “ALIS: An Affinity Selection-Mass Spectrometry System for the Discovery and Characterization of Protein-Ligand Interactions” D. A. Annis, C.-C. Chuang, and N. Nazef. In Mass Spectrometry in Medicinal Chemistry. Edited by Wanner K, Hofner G: Wiley-VCH; 2007:121-184. Mannhold R, Kubinyi H, Folkers G (Series Editors): Methods and Principles in Medicinal Chemistry.

Binding Assays in Intact Cells

It is possible to measure binding of peptides or peptidomimetic macrocycles to their natural acceptors in intact cells by immunoprecipitation experiments. For example, intact cells are incubated with fluoresceinated (FITC-labeled) compounds for 4 hrs in the absence of serum, followed by serum replacement and further incubation that ranges from 4-18 hrs. Cells are then pelleted and incubated in lysis buffer (50 mM Tris [pH 7.6], 150 mM NaCl, 1% CHAPS and protease inhibitor cocktail) for 10 minutes at 4° C. Extracts are centrifuged at 14,000 rpm for 15 minutes and supernatants collected and incubated with 10 μl goat anti-FITC antibody for 2 hrs, rotating at 4° C. followed by further 2 hrs incubation at 4° C. with protein A/G Sepharose (50 μl of 50% bead slurry). After quick centrifugation, the pellets are washed in lysis buffer containing increasing salt concentration (e.g., 150, 300, 500 mM). The beads are then re-equilibrated at 150 mM NaCl before addition of SDS-containing sample buffer and boiling. After centrifugation, the supernatants are optionally electrophoresed using 4%-12% gradient Bis-Tris gels followed by transfer into Immobilon-P membranes. After blocking, blots are optionally incubated with an antibody that detects FITC and also with one or more antibodies that detect proteins that bind to the peptidomimetic macrocycle.

Cellular Penetrability Assays

A peptidomimetic macrocycle is, for example, more cell penetrable compared to a corresponding uncrosslinked macrocycle. Peptidomimetic macrocycles with optimized linkers possess, for example, cell penetrability that is at least two-fold greater than a corresponding uncrosslinked macrocycle, and often 20% or more of the applied peptidomimetic macrocycle will be observed to have penetrated the cell after 4 hours. To measure the cell penetrability of peptidomimetic macrocycles and corresponding uncrosslinked macrocycle, intact cells are incubated with fluorescently-labeled (e.g. fluoresceinated) peptidomimetic macrocycles or corresponding uncrosslinked macrocycle (10 μM) for 4 hrs in serum free media at 37° C., washed twice with media and incubated with trypsin (0.25%) for 10 min at 37° C. The cells are washed again and resuspended in PBS. Cellular fluorescence is analyzed, for example, by using either a FACSCalibur flow cytometer or Cellomics' KineticScan® HCS Reader.

Cellular Efficacy Assays

The efficacy of certain peptidomimetic macrocycles is determined, for example, in cell-based killing assays using a variety of tumorigenic and non-tumorigenic cell lines and primary cells derived from human or mouse cell populations. Cell viability is monitored, for example, over 24-96 hrs of incubation with peptidomimetic macrocycles (0.5 to 50 μM) to identify those that kill at EC₅₀<10 μM. Several standard assays that measure cell viability are commercially available and are optionally used to assess the efficacy of the peptidomimetic macrocycles. In addition, assays that measure Annexin V and caspase activation are optionally used to assess whether the peptidomimetic macrocycles kill cells by activating the apoptotic machinery. For example, the Cell Titer-glo assay is used which determines cell viability as a function of intracellular ATP concentration.

In Vivo Stability Assay

To investigate the in vivo stability of the peptidomimetic macrocycles, the compounds are, for example, administered to mice and/or rats by IV, IP, PO or inhalation routes at concentrations ranging from 0.1 to 50 mg/kg and blood specimens withdrawn at 0′, 5′, 15′, 30′, 1 hr, 4 hrs, 8 hrs and 24 hours post-injection. Levels of intact compound in 25 μL of fresh serum are then measured by LC-MS/MS as above.

In Vivo Efficacy in Animal Models

To determine the anti-oncogenic activity of peptidomimetic macrocycles in vivo, the compounds are, for example, given alone (IP, IV, PO, by inhalation or nasal routes) or in combination with sub-optimal doses of relevant chemotherapy (e.g., cyclophosphamide, doxorubicin, etoposide). In one example, 5×10⁶ RS4;11 cells (established from the bone marrow of a patient with acute lymphoblastic leukemia) that stably express luciferase are injected by tail vein in NOD-SCID mice 3 hrs after they have been subjected to total body irradiation. If left untreated, this form of leukemia is fatal in 3 weeks in this model. The leukemia is readily monitored, for example, by injecting the mice with D-luciferin (60 mg/kg) and imaging the anesthetized animals (e.g., Xenogen In Vivo Imaging System, Caliper Life Sciences, Hopkinton, Mass.). Total body bioluminescence is quantified by integration of photonic flux (photons/sec) by Living Image Software (Caliper Life Sciences, Hopkinton, Mass.). Peptidomimetic macrocycles alone or in combination with sub-optimal doses of relevant chemotherapeutics agents are, for example, administered to leukemic mice (10 days after injection/day 1 of experiment, in bioluminescence range of 14-16) by tail vein or IP routes at doses ranging from 0.1 mg/kg to 50 mg/kg for 7 to 21 days. Optionally, the mice are imaged throughout the experiment every other day and survival monitored daily for the duration of the experiment. Expired mice are optionally subjected to necropsy at the end of the experiment. Another animal model is implantation into NOD-SCID mice of DoHH2, a cell line derived from human follicular lymphoma, that stably expresses luciferase. These in vivo tests optionally generate preliminary pharmacokinetic, pharmacodynamic and toxicology data.

Clinical Trials

To determine the suitability of the peptidomimetic macrocycles for treatment of humans, clinical trials are performed. For example, patients diagnosed with solid tumor and in need of treatment can be selected and separated in treatment and one or more control groups, wherein the treatment group is administered a peptidomimetic macrocycle, while the control groups receive a placebo or a known anti-cancer drug. The treatment safety and efficacy of the peptidomimetic macrocycles can thus be evaluated by performing comparisons of the patient groups with respect to factors such as survival and quality-of-life. In this example, the patient group treated with a peptidomimetic macrocycle can show improved long-term survival compared to a patient control group treated with a placebo.

Formulation and Administration Mode of Administration

An effective amount of a peptidomimetic macrocycles or a pharmaceutically acceptable salt thereof of the disclosure can be administered in a pharmaceutical composition, as either single or multiple doses by an accepted mode of administration. In some embodiments, a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, of the disclosure are administered parenterally, for example, by subcutaneous, intramuscular, intrathecal, intravenous or epidural injection. For example, a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof is administered intravenously, intraarterially, subcutaneously or by infusion. In some examples, a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof is administered intravenously. In some examples, a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof is administered intraarterially.

Regardless of the route of administration selected, the peptidomimetic macrocycles of the present disclosure, and/or the pharmaceutical compositions of the present disclosure, are formulated into pharmaceutically-acceptable dosage forms by conventional methods known to those of skill in the art. The peptidomimetic macrocycles according to the disclosure can be formulated for administration in any convenient way for use in human or veterinary medicine, by analogy with other pharmaceuticals.

In one aspect, the disclosure provides pharmaceutical composition comprising a therapeutically-effective amount of one or more of the peptidomimetic macrocycles described above, formulated together with one or more pharmaceutically acceptable carriers (additives) and/or diluents. In one embodiment, one or more of the peptidomimetic macrocycles described herein are formulated for parenteral administration for parenteral administration, one or more peptidomimetic macrocycles disclosed herein can be formulated as aqueous or nonaqueous solutions, dispersions, suspensions or emulsions or sterile powders which can be reconstituted into sterile injectable solutions or dispersions just prior to use. Such a pharmaceutical composition can comprise sugars, alcohols, antioxidants, buffers, bacteriostats, solutes which render the formulation isotonic with the blood of the intended recipient or suspending or thickening agents. A pharmaceutical composition can also contain adjuvants such as preservatives, wetting agents, emulsifying agents and dispersing agents. Prevention of the action of microorganisms upon the subject compounds can be ensured by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol sorbic acid, and the like. It can also be desirable to include isotonic agents, such as sugars, sodium chloride, and the like into a pharmaceutical composition. In addition, prolonged absorption of an injectable pharmaceutical composition can be brought about by the inclusion of agents which delay absorption such as aluminum monostearate and gelatin. If desired a pharmaceutical composition can be diluted prior to use with, for example, an isotonic saline solution or a dextrose solution. In some examples, the peptidomimetic macrocycle is formulated as an aqueous solution and is administered intravenously.

Amount and Frequency of Administration

Dosing can be determined using techniques known to one skilled in the art. The selected dosage level can depend upon a variety of factors including the activity of the particular peptidomimetic macrocycle employed, the route of administration, the time of administration, the rate of excretion or metabolism of the particular peptidomimetic macrocycle being employed, the duration of the treatment, other drugs, compounds and/or materials used in combination with the particular peptidomimetic macrocycle employed, the age, sex, weight, condition, general health and prior medical history of the patient being treated, and like factors well known in the medical arts. The dosage values can also vary with the severity of the condition to be alleviated. For any particular subject, specific dosage regimens can be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions.

A physician or veterinarian having ordinary skill in the art can readily determine and prescribe the effective amount of the pharmaceutical composition required. For example, the physician or veterinarian could start doses of the compounds of the disclosure employed in the pharmaceutical composition at levels lower than that required in order to achieve the desired therapeutic effect and gradually increase the dosage until the desired effect is achieved.

In some embodiments, a suitable daily dose of a peptidomimetic macrocycle of the disclosure can be that amount of the peptidomimetic macrocycle which is the lowest dose effective to produce a therapeutic effect. Such an effective dose will generally depend upon the factors described above. The precise time of administration and amount of any particular peptidomimetic macrocycle that will yield the most effective treatment in a given patient will depend upon the activity, pharmacokinetics, and bioavailability of a particular peptidomimetic macrocycle, physiological condition of the patient (including age, sex, disease type and stage, general physical condition, responsiveness to a given dosage and type of medication), route of administration, and the like.

Dosage can be based on the amount of the peptidomimetic macrocycle per kg body weight of the patient. Other amounts are known to those of skill in the art and readily determined. Alternatively, the dosage of the subject disclosure can be determined by reference to the plasma concentrations of the peptidomimetic macrocycle. For example, the maximum plasma concentration (Cmax) and the area under the plasma concentration-time curve from time 0 to infinity (AUC) can be used.

In some embodiment, the subject is a human subject and the amount of the peptidomimetic macrocycle administered is 0.01-100 mg per kilogram body weight of the human subject. For example, in various examples, the amount of the peptidomimetic macrocycle administered is about 0.01-50 mg/kg, about 0.01-20 mg/kg, about 0.01-10 mg/kg, about 0.1-100 mg/kg, about 0.1-50 mg/kg, about 0.1-20 mg/kg, about 0.1-10 mg/kg, about 0.5-100 mg/kg, about 0.5-50 mg/kg, about 0.5-20 mg/kg, about 0.5-10 mg/kg, about 1-100 mg/kg, about 1-50 mg/kg, about 1-20 mg/kg, about 1-10 mg/kg body weight of the human subject. In one embodiment, about 0.5 mg-10 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject is administered. In some examples the amount of the peptidomimetic macrocycle administered is about 0.16 mg, 0.32 mg, 0.64 mg, 1.28 mg, 3.56 mg, 7.12 mg, 14.24, or 20 mg per kilogram body weight of the human subject. In some examples the amount of the peptidomimetic macrocycle administered is about 0.16 mg, 0.32 mg, 0.64 mg, 1.28 mg, 3.56 mg, 7.12 mg, or 14.24 mg per kilogram body weight of the human subject. In some examples the amount of the peptidomimetic macrocycle administered is 0.16 mg per kilogram body weight of the human subject. In some examples the amount of the peptidomimetic macrocycle administered is 0.32 mg per kilogram body weight of the human subject. In some examples the amount of the peptidomimetic macrocycle administered is 0.64 mg per kilogram body weight of the human subject. In some examples the amount of the peptidomimetic macrocycle administered is 1.28 mg per kilogram body weight of the human subject. In some examples the amount of the peptidomimetic macrocycle administered is 3.56 mg per kilogram body weight of the human subject. In some examples the amount of the peptidomimetic macrocycle administered is 7.12 mg per kilogram body weight of the human subject. In some examples the amount of the peptidomimetic macrocycle administered is 14.24 mg per kilogram body weight of the human subject.

In some embodiments about 0.5-20 mg or 0.5-10 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject is administered two times a week. For example about 0.5-1.0 mg, 0.5-5.0 mg, 0.5-10.0 mg, 0.5-15 mg, or 1-5 mg, 1-10 mg, 1-15 mg, 1-20 mg, 5-10 mg, 1-15 mg, 5-20 mg, 10-15 mg, 10-20 mg, 15-20 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject is administrated about twice a week. In some examples about 1.0 mg, 1.25 mg, 1.5 mg, 1.75 mg, 2.0 mg, 2.25 mg, 2.5 mg, 2.75 mg, 3.0 mg, 3.25 mg, 3.5 mg, 3.75 mg, 4.0 mg, 4.25 mg, 4.5 mg, 4.75 mg, 5.0 mg, 5.25 mg, 5.5 mg, 5.75 mg, 6.0 mg, 6.25 mg, 6.5 mg, 6.75 mg, 7.0 mg, 7.25 mg, 7.5 mg, 7.75 mg, 8.0 mg, 8.25 mg, 8.5 mg, 8.75 mg, 9.0 mg, 9.25 mg, 9.5 mg, 9.75 mg, 10.0 mg, 10.25 mg, 10.5 mg, 10.75 mg, 11.0 mg, 11.25 mg, 11.5 mg, 11.75 mg, 12.0 mg, 12.25 mg, 12.5 mg, 12.75 mg, 13.0 mg, 13.25 mg, 13.5 mg, 13.75 mg, 14.0 mg, 14.25 mg, 14.5 mg, 14.75 mg, 15.0 mg, 15.25 mg, 15.5 mg, 15.75 mg, 16.0 mg, 16.5 mg, 17.0 mg, 17.5 mg, 18.0 mg, 18.5 mg, 19.0 mg, 19.5 mg, or 20.0 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject is administered two times a week. In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg, 10.0, or 20 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered two times a week. In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg or 10.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered two times a week.

In some embodiments about 0.5-20 mg or 0.5-10 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject is administered once a week. For example about 0.5-1.0 mg, 0.5-5.0 mg, 0.5-10.0 mg, 0.5-15 mg, or 1-5 mg, 1-10 mg, 1-15 mg, 1-20 mg, 5-10 mg, 1-15 mg, 5-20 mg, 10-15 mg, 10-20 mg, 15-20 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject is administrated once a week. In some examples about 1.0 mg, 1.25 mg, 1.5 mg, 1.75 mg, 2.0 mg, 2.25 mg, 2.5 mg, 2.75 mg, 3.0 mg, 3.25 mg, 3.5 mg, 3.75 mg, 4.0 mg, 4.25 mg, 4.5 mg, 4.75 mg, 5.0 mg, 5.25 mg, 5.5 mg, 5.75 mg, 6.0 mg, 6.25 mg, 6.5 mg, 6.75 mg, 7.0 mg, 7.25 mg, 7.5 mg, 7.75 mg, 8.0 mg, 8.25 mg, 8.5 mg, 8.75 mg, 9.0 mg, 9.25 mg, 9.5 mg, 9.75 mg, 10.0 mg, 10.25 mg, 10.5 mg, 10.75 mg, 11.0 mg, 11.25 mg, 11.5 mg, 11.75 mg, 12.0 mg, 12.25 mg, 12.5 mg, 12.75 mg, 13.0 mg, 13.25 mg, 13.5 mg, 13.75 mg, 14.0 mg, 14.25 mg, 14.5 mg, 14.75 mg, 15.0 mg, 15.25 mg, 15.5 mg, 15.75 mg, 16.0 mg, 16.5 mg, 17.0 mg, 17.5 mg, 18.0 mg, 18.5 mg, 19.0 mg, 19.5 mg, or 20.0 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject is administered once a week. In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg 10.0 mg, or 20.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered once a week. In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg or 10.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered once a week

In some embodiments about 0.5-20 mg or 0.5-10 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject is administered 3, 4, 5, 6 or 7 times a week. For example about 0.5-1.0 mg, 0.5-5.0 mg, 0.5-10.0 mg, 0.5-15 mg, or 1-5 mg, 1-10 mg, 1-15 mg, 1-20 mg, 5-10 mg, 1-15 mg, 5-20 mg, 10-15 mg, 10-20 mg, 15-20 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject is administrated 3, 4, 5, 6, or 7 times a week. In some examples about 1.0 mg, 1.25 mg, 1.5 mg, 1.75 mg, 2.0 mg, 2.25 mg, 2.5 mg, 2.75 mg, 3.0 mg, 3.25 mg, 3.5 mg, 3.75 mg, 4.0 mg, 4.25 mg, 4.5 mg, 4.75 mg, 5.0 mg, 5.25 mg, 5.5 mg, 5.75 mg, 6.0 mg, 6.25 mg, 6.5 mg, 6.75 mg, 7.0 mg, 7.25 mg, 7.5 mg, 7.75 mg, 8.0 mg, 8.25 mg, 8.5 mg, 8.75 mg, 9.0 mg, 9.25 mg, 9.5 mg, 9.75 mg, 10.0 mg, 10.25 mg, 10.5 mg, 10.75 mg, 11.0 mg, 11.25 mg, 11.5 mg, 11.75 mg, 12.0 mg, 12.25 mg, 12.5 mg, 12.75 mg, 13.0 mg, 13.25 mg, 13.5 mg, 13.75 mg, 14.0 mg, 14.25 mg, 14.5 mg, 14.75 mg, 15.0 mg, 15.25 mg, 15.5 mg, 15.75 mg, 16.0 mg, 16.5 mg, 17.0 mg, 17.5 mg, 18.0 mg, 18.5 mg, 19.0 mg, 19.5 mg, or 20.0 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject is administered 3, 4, 5, 6, or 7 times a week. In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg 10.0 mg, or 20.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered 3, 4, 5, 6, or 7 times a week. In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg or 10.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered 3, 4, 5, 6, or 7 times a week.

In some embodiments about 0.5-20 mg or 0.5-10 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject is administered once every 2, 3, or 4 weeks. For example about 0.5-1.0 mg, 0.5-5.0 mg, 0.5-10.0 mg, 0.5-15 mg, or 1-5 mg, 1-10 mg, 1-15 mg, 1-20 mg, 5-10 mg, 1-15 mg, 5-20 mg, 10-15 mg, 10-20 mg, 15-20 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject is administrated 3, 4, 5, 6, or 7 once every 2 or 3 week. In some examples about 1.0 mg, 1.25 mg, 1.5 mg, 1.75 mg, 2.0 mg, 2.25 mg, 2.5 mg, 2.75 mg, 3.0 mg, 3.25 mg, 3.5 mg, 3.75 mg, 4.0 mg, 4.25 mg, 4.5 mg, 4.75 mg, 5.0 mg, 5.25 mg, 5.5 mg, 5.75 mg, 6.0 mg, 6.25 mg, 6.5 mg, 6.75 mg, 7.0 mg, 7.25 mg, 7.5 mg, 7.75 mg, 8.0 mg, 8.25 mg, 8.5 mg, 8.75 mg, 9.0 mg, 9.25 mg, 9.5 mg, 9.75 mg, 10.0 mg, 10.25 mg, 10.5 mg, 10.75 mg, 11.0 mg, 11.25 mg, 11.5 mg, 11.75 mg, 12.0 mg, 12.25 mg, 12.5 mg, 12.75 mg, 13.0 mg, 13.25 mg, 13.5 mg, 13.75 mg, 14.0 mg, 14.25 mg, 14.5 mg, 14.75 mg, 15.0 mg, 15.25 mg, 15.5 mg, 15.75 mg, 16.0 mg, 16.5 mg, 17.0 mg, 17.5 mg, 18.0 mg, 18.5 mg, 19.0 mg, 19.5 mg, or 20.0 mg of the peptidomimetic macrocycle per kilogram body weight of the human subject is administered once every 2 or 3 weeks. In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg 10.0 mg, or 20.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered once every 2 weeks. In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg or 10.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered once every 2 weeks. In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg 10.0 mg, or 20.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered once every 3 weeks. In some examples, the amount of the peptidomimetic macrocycle administered is about 1.25 mg, 2.5 mg, 5.0 mg or 10.0 mg per kilogram body weight of the human subject and the peptidomimetic macrocycle is administered once every 3 weeks.

In some embodiments, the peptidomimetic macrocycle is administered gradually over a period of time. A desired amount of peptidomimetic macrocycle can be administered gradually over a period of from about 0.1 h-24 h. In some cases a desired amount of peptidomimetic macrocycle is administered gradually over a period of 0.1 h, 0.5 h, 1 h, 1.5 h, 2 h, 2.5 h, 3 h, 3.5 h, 4 h, 4.5 h, 5 h, 6 h, 7 h, 8 h, 9 h, 10 h, 11 h, 12 h, 13 h, 14 h, 15 h, 16 h, 17 h, 18 h, 19 h, 20 h, 21 h, 22 h, 23 h, or 24 h. In some examples, a desired amount of peptidomimetic macrocycle is administered gradually over a period of 0.25-12 h, for example over a period of 0.25-1 h, 0.25-2 h, 0.25-3 h, 0.25-4 h, 0.25-6 h, 0.25-8 h, 0.25-10 h. In some examples, a desired amount of peptidomimetic macrocycle is administered gradually over a period of 0.25-2 h. In some examples, a desired amount of peptidomimetic macrocycle is administered gradually over a period of 0.25-1 h. In some examples, a desired amount of peptidomimetic macrocycle is administered gradually over a period of 0.25 h, 0.3 h, 0.4 h, 0.5 h, 0.6 h, 0.7 h, 0.8 h, 0.9 h, 1.0 h, 1.1 h, 1.2 h, 1.3 h, 1.4 h, 1.5 h, 1.6 h, 1.7 h, 1.8 h, 1.9 h, or 2.0 h. In some examples, a desired amount of peptidomimetic macrocycle is administered gradually over a period of 1 h. In some examples, a desired amount of peptidomimetic macrocycle is administered gradually over a period of 2 h.

Administration of the peptidomimetic macrocycles can continue as long as necessary to treat a solid tumor in a subject in need thereof. In some embodiments, one or more peptidomimetic macrocycle of the disclosure is administered for more than 1 day, 1 week, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, 13 months, 14 months, 15 months, 16 months, 17 months, 18 months, 19 months, 20 months, 21 months, 22 months, 23 months, or 24 months. In some embodiments, one or more peptidomimetic macrocycle of the disclosure is administered for less than 1 week, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, 13 months, 14 months, 15 months, 16 months, 17 months, 18 months, 19 months, 20 months, 21 months, 22 months, 23 months, or 24 months.

In some embodiments, the peptidomimetic macrocycle is administered on day 1, 8, 15 and 28 of a 28 day cycle. In some embodiments, the peptidomimetic macrocycle is administered on day 1, 8, 15 and 28 of a 28 day cycle and administration is continued for two cycles. In some embodiments, the peptidomimetic macrocycle is administered on day 1, 8, 15 and 28 of a 28 day cycle and administration is continued for three cycles. In some embodiments, the peptidomimetic macrocycle is administered on day 1, 8, 15 and 28 of a 28 day cycle and administration is continued for 4, 5, 6, 7, 8, 9, 10, or more cycles.

In some embodiments, one or more peptidomimetic macrocycle of the disclosure is administered chronically on an ongoing basis. In some embodiments administration of one or more peptidomimetic macrocycle of the disclosure is continued until documentation of disease progression, unacceptable toxicity, or patient or physician decision to discontinue administration.

Method and Uses

In one aspect, the disclosure provides a method of treating solid tumor in a subject, the method comprising administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins. In some embodiments, the peptidomimetic macrocycle can disrupt the interaction between p53 and MDM2 and MDMX. In some embodiments, treatment according to the method disclosed herein can result in re-activation of the p53 pathway, decreased tumor cell proliferation, increased p53 protein, increased p21, and/or increased apoptosis in the human subject.

In one aspect, the disclosure provides a method of treating solid tumor, that lacks a p53 deactivating mutation, in a subject the method comprising administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins. In some embodiments, the solid tumor is determined to lack a p53 mutation prior to treatment In some embodiments, the peptidomimetic macrocycle can disrupt the interaction between p53 and MDM2 and MDMX. The method further can comprise confirming the lack of the p53 deactivating mutation in the subject prior to the administration of the peptidomimetic macrocycle. In some embodiments, treatment according to the method disclosed herein can result in re-activation of the p53 pathway, decreased tumor cell proliferation, increased p53 protein, increased p21, and/or increased apoptosis in the human subject.

In one aspect, the disclosure provides a method of treating solid tumor in a subject expressing wild type p53, the method comprising administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins. In some embodiments, the peptidomimetic macrocycle can disrupt the interaction between p53 and MDM2 and MDMX. The method further can comprise confirming the wild type p53 status of the subject prior to the administration of the peptidomimetic macrocycle. In some embodiments, treatment according to the method disclosed herein can result in re-activation of the p53 pathway, decreased tumor cell proliferation, increased p53 protein, increased p21, and/or increased apoptosis in the human subject.

In some embodiments, the methods for treating solid tumor provided herein inhibit, reduce, diminish, arrest, or stabilize a tumor associated with the solid tumor. In other embodiments, the methods for treating solid tumor provided herein inhibit, reduce, diminish, arrest, or stabilize the blood flow, metabolism, or edema in a tumor associated with the solid tumor or one or more symptoms thereof. In some examples, the methods for treating solid tumor provided herein cause the regression of a tumor, tumor blood flow, tumor metabolism, or peritumor edema, and/or one or more symptoms associated with the solid tumor. In other examples, the methods for treating solid tumor provided herein maintain the size of the tumor so that it does not increase, or so that it increases by less than the increase of a tumor after administration of a standard therapy as measured by conventional methods available to one of skill in the art, such as ultrasound, CT Scan, MRI, dynamic contrast-enhanced MRI, or PET Scan. In some examples, the methods for treating solid tumor provided herein decrease tumor size. In some examples, the methods for treating solid tumor provided herein reduce the formation of a tumor. In some examples, the methods for treating solid tumor provided herein eradicate, remove, or control primary, regional and/or metastatic tumors associated with the solid tumor. In some examples, the methods for treating solid tumor provided herein decrease the number or size of metastases associated with the solid tumor. In some examples, the methods for treating solid tumor provided herein reduce the tumor volume or tumor size (e.g., diameter) in a subject by an amount in the range of about 5-10%, 5-20%, 10-20%, 15-20%, 10-30%, 20-30%, 20-40%, 30-40%, 10-50%, 20-50%, 30-50%, 40-50%, 10-60%, 20-60%, 30-60%, 40-60%, 50-60%, 10-70%, 20-70%, 30-70%, 40-70%, 50-70%, 60-70%, 10-80%, 20-80%, 30-80%, 40-80%, 50-80%, 60-80%, 70-80%, 10-90%, 20-90%, 30-90%, 40-90%, 50-90%, 60-90%, 70-90%, 80-90%, 10-100%, 20%-100%, 30- 100%, 40-100%, 50-100%, 60-100%, 70-100%, 80-100%, 90-100%, 95-100%, or any range in between, relative to tumor size (e.g., volume or diameter) in a subject prior to administration of the peptidomimetic macrocycles as assessed by methods well known in the art, e.g., CT Scan, MRI, DCE-MRI, or PET Scan. In certain embodiments, the methods herein reduce the tumor size (e.g., volume or diameter) in a subject by at least about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 80%, 85%, 90%, 95%, 99%, or 100%, relative to tumor volume or tumor size (e.g., diameter) prior to administration of the peptidomimetic macrocycle as assessed by methods well known in the art, e.g., CT Scan, MRI, DCE-MRI, or PET Scan.

In some embodiments, the methods provided herein reduce the tumor perfusion in a subject by an amount in the range of about 5-10%, 5-20%, 10-20%, 15-20%, 10-30%, 20-30%, 20-40%, 30-40%, 10-50%, 20-50%, 30-50%, 40-50%, 10-60%, 20-60%, 30-60%, 40-60%, 50-60%, 10-70%, 20-70%, 30-70%, 40-70%, 50-70%, 60-70%, 10-80%, 20-80%, 30-80%, 40-80%, 50-80%, 60-80%, 70-80%, 10-90%, 20-90%, 30-90%, 40-90%, 50-90%, 60-90%, 70-90%, 80-90%, 10-100%, 20%-100%, 30-100%, 40-100%, 50-100%, 60-100%, 70-100%, 80-100%, 90-100%, 95-100%, or any range in between, relative to tumor perfusion prior to administration of the peptidomimetic macrocycle, as assessed by methods well known in the art, e.g., MRI, DCE-MRI, or PET Scan. In certain embodiments, the methods provided herein reduce the tumor perfusion in a subject by at least about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 80%, 85%, 90%, 95%, 99%, or 100%, relative to tumor perfusion prior to administration of the peptidomimetic macrocycle as assessed by methods well known in the art, e.g., MRI, DCE-MRI, or PET Scan.

In some embodiments, the methods provided herein inhibit or decrease tumor metabolism in a subject in the range of about 5-10%, 5-20%, 10-20%, 15-20%, 10-30%, 20-30%, 20-40%, 30-40%, 10-50%, 20-50%, 30-50%, 40-50%, 10-60%, 20-60%, 30-60%, 40-60%, 50-60%, 10-70%, 20-70%, 30-70%, 40-70%, 50-70%, 60-70%, 10-80%, 20-80%, 30-80%, 40-80%, 50-80%, 60-80%, 70-80%, 10-90%, 20-90%, 30-90%, 40-90%, 50-90%, 60-90%, 70-90%, 80-90%, 10-100%, 20%-100%, 30-100%, 40-100%, 50-100%, 60-100%, 70-100%, 80-100%, 90-100%, 95-100%, or any range in between, relative to tumor metabolism prior to administration of the peptidomimetic macrocycle, as assessed by methods well known in the art. In certain embodiments, the methods provided herein inhibit or decrease tumor metabolism in a subject as assessed by methods well known in the art, e.g., PET scanning. In specific embodiments, the methods provided herein inhibit or decrease tumor metabolism in a subject by at least about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 80%, 85%, 90%, 95%, or 100%, relative to tumor metabolism prior to administration of the peptidomimetic macrocycle, as assessed by methods well known in the art.

In other aspect, the disclosure provides a method for increasing the survival time of a subject with solid tumor determined to lack a p53 deactivating mutation and/or with solid tumor expressing wild type p53, the method comprising administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins. In some examples, the survival time of the subject is at least 30 days longer than the expected survival time of the subject if the subject was not treated according to the methods provided herein. In some examples, the survival time of the subject is at 1 month-about 5 years longer than the expected survival time of the subject if the subject was not treated according to the methods provided herein. For example, the survival time of the subject is at least 3 months, at least 6 months, at least 9 months, at least 12 months, at least 15 months, at least 18 months, at least 21 months, or at least 24 months longer than the expected survival time of the subject if the subject was not treated according to the methods disclosed herein disclosure.

In one aspect, the disclosure provides a method to access presence, absence or amount of the biomarker biomarkers in a subject suffering with solid tumor, the method comprising. In some examples, the biomarkers include patient biomarkers for example the p53 status of the subject and the MDM2 and MDMX expression levels in the subject.

The method of the disclosure can also optionally include studying and/or evaluating the safety and/or tolerability of the peptidomimetic macrocycles disclosed herein in the subject.

Also provided herein is a method to re-activate the p53 pathway in a subject with a solid tumor lacking a p53 deactivating mutation and/or expressing wild type p53, the method comprising administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins.

Also provided herein is a method to decrease tumor cell proliferation in a human subject with a solid tumor lacking a p53 deactivating mutation and/or expressing wild type p53, the method comprising administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins.

Also provided herein is a method to increased p53 protein in a subject with a solid tumor lacking a p53 deactivating mutation and/or expressing wild type p53, the method comprising administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins.

Also provided herein is a method to increased p21 in a subject with a solid tumor lacking a p53 deactivating mutation and/or expressing wild type p53, the method comprising administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins.

Also provided herein is a method to increased apoptosis in a subject with a solid tumor lacking a p53 deactivating mutation and/or expressing wild type p53, the method comprising administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins.

In some embodiments, the disclosure also provides a method to determine the dose limiting toxicities (DLTs) and/or maximum tolerated dose (MTD) of the peptidomimetic macrocycles disclosed herein in subject with a solid tumor lacking a p53 deactivating mutation and/or expressing wild type p53.

The methods of the disclosure can optionally include pharmacokinetic analysis of the peptidomimetic macrocycles disclosed herein. Accordingly, the methods can further comprise collecting one or more biological sample from the subject at one or more specific time point and analyzing the one or more biological sample for levels of the peptidomimetic macrocycles and/or it metabolites. The biological sample can be a blood sample from the subject, for example blood sample from a human subject. The one or more specific time point can include time points before, after and/or during the administration of the peptidomimetic macrocycle to the subject. In some embodiments one or more biological sample includes biological samples collected before and after each administration of the peptidomimetic macrocycle to the subject. In some embodiments a biological sample for pharmacokinetic analysis is collected before the first administration of the peptidomimetic macrocycle to the subject and at one or more time points after each administration of the peptidomimetic macrocycles to the subject. The biological sample collected before the administration of the peptidomimetic macrocycle to the subject can be done within 0-24 hour before the start of administration of the peptidomimetic macrocycle to the subject. For example, the biological sample can be collected within 24 h, 23 h, 22 h, 21 h, 20 h, 19 h, 18 h, 17 h, 16 h, 15 h, 14 h, 13 h, 12 h, 11 h, 10 h, 9 h, 8 h, 7 h, 6 h, 5 h, 4 h, 3 h, 2 h, 1 h, 30 min, 15 min, or immediately before the administration of the peptidomimetic macrocycle to the subject. One or more biological samples collected after the administration of the peptidomimetic macrocycle to the subject can be collected from 0-about 72 h, for example after 0 min, 5 min, 10 min, 20 min, 30 min, 45 min, 60 min, 1.25 h, 1.5 h, 1.75 h, 2.0 h, 2.25 h, 2.5 h, 2.75 h, 3.0 h, 3.25 h, 3.5 h, 3.75 h, 4.0 h, 4.25 h, 4.5 h, 4.75 h, 5.0 h, 5.25 h, 5.5 h, 5.75 h, 6.0 h, 6.25 h, 6.5 h, 6.75 h, 7.0 h, 7.25 h, 7.5 h, 7.75 h, 8.0 h, 8.25 h, 8.5 h, 8.75 h, 9.0 h, 9.25 h, 9.5 h, 9.75 h, 10.0 h, 10.25 h, 10.5 h, 10.75 h, 11.0 h, 11.25 h, 11.5 h, 11.75 h, 12.0 h, 20 h, 24 h, 28 h, 32 h, 36 h, 40 h, 44 h, 48 h, 52 h, 56 h, 60 h, 64 h, 68 h, or 72 h after the administration of the peptidomimetic macrocycle to the subject. In some embodiments, the peptidomimetic macrocycle is administered on day 1, day 8, day 15 of a 28 day cycle and biological sample is collected before administration on day 1, after the administration on day 1 (multiple biological samples can be collected, for example after about 0 min, about 30 min, about 1 h, about 2 h, about 4 h, about 8 h, about 24 h, and 48 hour after administration), before administration on day 8, after administration on day 8 (multiple biological samples can be collected, for example after about 0 min, about 30 min, about 1 h, about 2 h, and about 4 h after administration), before administration on day 15 and after administration on day 15 (multiple biological samples can be collected, for example after about 0 min, about 30 min, about 1 h, about 2 h, about 4 h, about 8 h, and about 24 h after administration).

The method of the disclosure can optionally include pharmacodynamic analysis of the peptidomimetic macrocycles disclosed herein. Accordingly, the methods can comprise collecting one or more biological samples from the subject at one or more specific time points for pharmacodynamic analysis. Pharmacodynamic analysis can include analyzing the levels of biomarkers including MIC-1, p53, MDM2, MDMX, p21 and/or cases in the biological sample. Detection of biomarkers in a biological sample can be performed by any conventional method for detecting the type of biomarker, e.g., direct measurement, immunohistochemistry, immunoblotting, immunoflourescense, immunoabsorbence, immunoprecipitations, protein array, flourescence in situ hybridization, FACS analysis, hybridization, in situ hybridization, Northern blots, Southern blots, Western blots, ELISA, radioimmunoassay, gene array/chip, PCR, RT-PCR, or cytogenetic analysis. The biological sample for pharmacodynamic analysis can be a blood sample or a tumor specimen from the subject, for example biological sample for pharmacodynamic analysis can be a blood sample or a tumor specimen from the human subject. The biological samples for pharmacodynamic analysis of the peptidomimetic macrocycles can be collected any time before, during, or after the administration of the peptidomimetic macrocycle to the subject. In some embodiments a blood sample for pharmacokinetic analysis is collected before the first administration of the peptidomimetic macrocycle to the subject and at one or more time points after each administration of the peptidomimetic macrocycles to the subject. The blood sample collected before the administration of the peptidomimetic macrocycle to the subject can be done within 0-24 hour before the start of administration of the peptidomimetic macrocycle to the subject. For example, the biological sample can be collected within 24 h, 23 h, 22 h, 21 h, 20 h, 19 h, 18 h, 17 h, 16 h, 15 h, 14 h, 13 h, 12 h, 11 h, 10 h, 9 h, 8 h, 7 h, 6 h, 5 h, 4 h, 3 h, 2 h, 1 h, 30 min, 15 min, or immediately before the administration of the peptidomimetic macrocycle to the subject. One or more blood samples for pharmacodynamic analysis collected after the administration of the peptidomimetic macrocycle to the subject can be collected from 0-about 72 h, for example after about 12 h, 24 h, 36 h or 48 h after the administration of the peptidomimetic macrocycle to the subject. In some embodiments, the peptidomimetic macrocycle is administered on day 1, day 8, day 15 of a 28 day cycle and blood samples for pharmacodynamic analysis are collected before administration on day 1, after the administration on day 1 (multiple samples can be collected, for example after about 24 h and 48 hour after administration), before administration on day 8, after administration on day 8 (multiple samples can be collected, for example with about 1 h administration), before administration on day 15 and after administration on day 15 (multiple samples can be collected, for example with about 1 h and about 48 h after administration), and day 22. Tumor specimens for pharmacodynamic analysis can be collected at any time before, after or during the administration of the peptidomimetic macrocycle to the subject. For example the peptidomimetic macrocycle can be administered on day 1, day 8, day 15 of a 28 day cycle and tumor samples for pharmacodynamic analysis are collected before administration on day 1 and between day 14-day 18, for example of day 16.

The method of the disclosure can optionally include clinical activity analysis of the peptidomimetic macrocycles disclosed herein. Accordingly, the methods can comprise analyzing one or more biological samples collected from the subject at one or more specific time points. Any appropriate analytical procedure can be used for the analysis of the biological samples. For example, imaging techniques like radiographs, ultrasound, CT scan, PET scan, MRI scan, chest x-ray, laparoscopy, complete blood count (CBC) test, bone scanning and fecal occult blood test can be used. Further analytical procedures that can be used include blood chemistry analysis, chromosomal translocation analysis, needle biopsy, tissue biopsy, fluorescence in situ hybridization, laboratory biomarker analysis, immunohistochemistry staining method, flow cytometry, or a combination thereof. The method can further comprise tabulating and/or plotting results of the analytical procedure.

Biological Samples

As used in the present application, “biological sample” means any fluid or other material derived from the body of a normal or diseased subject, such as blood, serum, plasma, lymph, urine, saliva, tears, cerebrospinal fluid, milk, amniotic fluid, bile, ascites fluid, pus, and the like. Also included within the meaning of the term “biological sample” is an organ or tissue extract and culture fluid in which any cells or tissue preparation from a subject has been incubated. Biological samples also include tumor samples or specimens. Tumor sample can be a tumor tissue sample. Methods of obtaining tumor tissue samples are well known in the art and can vary according to the type and location of a tumor and preferences of the physician. In some embodiments, the tumor tissue sample can obtained from surgically excised tissue. Tissue samples and cellular samples can also be obtained without invasive surgery, for example by punctuating the chest wall or the abdominal wall or from masses of breast, thyroid or other sites with a fine needle and withdrawing cellular material (fine needle aspiration biopsy).

The biological samples obtained can be used in fresh, frozen, or fixed (e.g., paraffin-embedded) form, depending on the nature of the sample, the assay used, and the convenience of the practitioner. Although fresh, frozen and fixed materials are suitable for various RNA and protein assays, generally, fresh tissues can be preferred for ex vivo measurements of activity.

Fixed tissue samples can also be employed. Tissue obtained by biopsy is often fixed, usually by formalin, formaldehyde, or gluteraldehyde, for example, or by alcohol immersion. Fixed biological samples are often dehydrated and embedded in paraffin or other solid supports, as is known in the art. See the reference Plenat et al., 2001, Ann. Pathol. 21:29-47. Non-embedded, fixed tissue, as well as fixed and embedded tissue, can be used in the present methods. Solid supports for embedding fixed tissue can be removed with organic solvents to enable subsequent rehydration of preserved tissue.

In some cases, the assay includes a step of cell or tissue culture. Culture methods are well known in the art. For example, cells from a biopsy can be disaggregated using enzymes (such as collagenase and hyaluronidase) and or physical disruption (e.g., repeated passage through a 25-gauge needle) to dissociate the cells, collected by centrifugation, and resuspended in desired buffer or culture medium for culture, immediate analysis, or further processing.

Subject/Patient Population

In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, who has or is diagnosed with a solid tumor. In other embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, predisposed or susceptible to a solid tumor. In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, at risk of developing a solid tumor.

In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, who has or is diagnosed with a solid tumor, determined to lack a p53 deactivating mutation and/or expressing wild type p53. In other embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, predisposed or susceptible to a solid tumor, determined to lack a p53 deactivating mutation and/or expressing wild type p53. In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, at risk of developing a solid tumor, determined to lack a p53 deactivating mutation and/or expressing wild type p53. A p53 deactivating mutation, as used herein is any mutation that leads to loss of (or a decrease in) the in vitro apoptotic activity of p53. Non limiting examples of p53 deactivating mutations are included in Table 1a. Accordingly, in some embodiments, a subject with a solid tumor in accordance with the composition as provided herein is a human who has or is diagnosed with a solid tumor that is determined to lack a p53 deactivation mutation, such as those shown in Table 1a.

In some embodiments, the subject treated for solid tumor in accordance with the methods provided herein is a human, who has or is diagnosed with a solid tumor, determined to have a p53 gain of function mutation. In other embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, predisposed or susceptible to a solid tumor, determined to have a p53 gain of function mutation. In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, at risk of developing a solid tumor, determined to have a p53 gain of function mutation. A p53 gain of function mutation, as used herein is any mutation such that the mutant p53 exerts oncogenic functions beyond their negative domination over the wild-type p53 tumor suppressor functions. The p53 gain of function mutant protein mat exhibit new activities that can contribute actively to various stages of tumor progression and to increased resistance to anticancer treatments. Non limiting examples of p53 gain of function mutation mutations are included in Table 1b. Accordingly, in some embodiments, a subject with a solid tumor in accordance with the composition as provided herein is a human who has or is diagnosed with a solid tumor that is determined to have a p53 gain of function mutation, such as those shown in Table 1b.

In some embodiments, the subject treated for solid tumor in accordance with the methods provided herein is a human, who has or is diagnosed with a solid tumor that is not p53 negative. In other embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, predisposed or susceptible to a solid tumor that is not p53 negative. In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, at risk of developing a solid tumor that is not p53 negative.

In some embodiments, the subject treated for solid tumor in accordance with the methods provided herein is a human, who has or is diagnosed with a solid tumor that expresses p53 with partial loss of function mutation. In other embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, predisposed or susceptible to a solid tumor that expresses p53 with partial loss of function mutation. In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, at risk of developing a solid tumor that expresses p53 with partial loss of function mutation. As used herein “a partial loss of p53 function” mutation means that the mutant p53 exhibits some level of function of normal p53, but to a lesser or slower extent. For example, a partial loss of p53 function can mean that the cells become arrested in cell division to a lesser or slower extent.

In some embodiments, the subject treated for solid tumor in accordance with the methods provided herein is a human, who has or is diagnosed with a solid tumor that expresses p53 with a copy loss mutation and a deactivating mutation. In other embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, predisposed or susceptible to a solid tumor that expresses p53 with a copy loss mutation and a deactivating mutation. In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, at risk of developing a solid tumor that expresses p53 with a copy loss mutation and a deactivating mutation.

In some embodiments, the subject treated for solid tumor in accordance with the methods provided herein is a human, who has or is diagnosed with a solid tumor that expresses p53 with a copy loss mutation. In other embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, predisposed or susceptible to a solid tumor that expresses p53 with a copy loss mutation. In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, at risk of developing a solid tumor that expresses p53 with a copy loss mutation.

In some embodiments, the subject treated for solid tumor in accordance with the methods provided herein is a human, who has or is diagnosed with a solid tumor that expresses p53 with one or more silent mutations. In other embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, predisposed or susceptible to a solid tumor that expresses p53 with one or more silent mutations. In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, at risk of developing a solid tumor that expresses p53 with one or more silent mutations. Silent mutations as used herein are mutations which cause no change in the encoded p53 amino acid sequence.

In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human, who has or is diagnosed with a solid tumor, determined to lack a dominant p53 deactivating mutation. Dominant p53 deactivating mutation or dominant negative mutation, as used herein, is a mutation wherein the mutated p53 inhibits or disrupt the activity of the wild-type p53 gene.

TABLE 1a Exemplary p53 deactivating mutations Mutation at position Amino acid change 62 E62_W91del 122 V122X 135 C135S 143 V143A 144 Q144P 146 W146X 157 V157F 158 R158H 163 Y163N 168 H168Y 173 V173L 175 R175H 175 R175P 175 R175Q 175 R175S 219 P219H 234 Y234C 234 Y234H 237 M237I 240 S240R 245 G245C 245 G245S 246 M246I 248 R248Q 248 R248W 249 R249S 272 V272M 273 R273H 274 V274F 279 G279E 280 R280K 281 D281H 282 R282W 306 R306P 308 P300_L308del 327 P300_Y327del 332 D324_I332del 337 R337C 344 L344P

TABLE 1b Exemplary p53 activating mutations AA position AAchange 46 S46F 121 S121F 123 T123A 288 N288K Table 1a and 1b refer to the sequence of the wild-type human TP53 tumor protein p53 shown in FIG. 1. Amino acid changes are reported as: the amino acid being substituted followed by the position of the amino acid being substituted in the wild type p53 sequence, followed by the amino acid used for substitution. For example L344P, indicates that the lysine (K) at the 344 position in the wild type sequence is replaced by a proline (P).

In some embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a refractory patient. In a certain embodiment, a refractory patient is a patient refractory to a standard therapy (e.g., surgery, radiation, anti-androgen therapy and/or drug therapy such as chemotherapy). In certain embodiments, a patient with the solid tumor is refractory to a therapy when the solid tumor has not significantly been eradicated and/or the one or more symptoms have not been significantly alleviated. The determination of whether a patient is refractory can be made either in vivo or in vitro by any method known in the art for assaying the effectiveness of a treatment of solid tumor. In various embodiments, a patient with solid tumor is refractory when one or more tumors associated with the solid tumor, have not decreased or have increased. In various embodiments, a patient with solid tumor is refractory when one or more tumors metastasize and/or spread to another organ.

In some embodiments, a subject treated for solid tumor accordance with the methods provided herein is a human that has proven refractory to therapies other than treatment with the peptidomimetic macrocycles of the disclosure, but is no longer on these therapies. In certain embodiments, a subject treated for solid tumor in accordance with the methods provided herein is a human already receiving one or more conventional anti-cancer therapies, such as surgery, drug therapy such as chemotherapy, anti-androgen therapy or radiation. Among these patients are refractory patients, patients who are too young for conventional therapies, and patients with recurring tumors despite treatment with existing therapies.

In some embodiments, the subject is a human who has had at least one unsuccessful prior treatment and/or therapy of the solid tumor.

Methods of Detecting Wild Type p53 and/or p53 Mutations

The tumor samples from a subject can be assayed in order to determine the lack of a p53 deactivating mutation and/or expression of wild type p53.

In order to detect the p53 wild-type gene and/or lack of p53 deactivation mutation in a tissue, it can be helpful to isolate the tissue free from surrounding normal tissues. Means for enriching a tissue preparation for tumor cells are known in the art. For example, the tissue can be isolated from paraffin or cryostat sections. Cancer cells can also be separated from normal cells by flow cytometry. These as well as other techniques for separating tumor from normal cells are well known in the art. If the tumor tissue is highly contaminated with normal cells, detection of mutations can be more difficult.

Detection of point mutations can be accomplished by molecular cloning of the p53 allele (or alleles) present in the tumor tissue and sequencing that allele(s) using techniques well known in the art. Alternatively, the polymerase chain reaction can be used to amplify p53 gene sequences directly from a genomic DNA preparation from the tumor tissue. The DNA sequence of the amplified sequences can then be determined. The polymerase chain reaction itself is well known in the art. See e.g., Saiki et al., Science, Vol. 239, p. 487, 1988; U.S. Pat. No. 4,683,202; and U.S. Pat. No. 4,683,195.

Specific deletions of p53 genes can also be detected. For example, restriction fragment length polymorphism (RFLP) probes for the p53 gene or surrounding marker genes can be used to score loss of a p53 allele. Other techniques for detecting deletions, as are known in the art can be used.

Loss of wild-type p53 genes can also be detected on the basis of the loss of a wild-type expression product of the p53 gene. Such expression products include both the mRNA as well as the p53 protein product itself. Point mutations can be detected by sequencing the mRNA directly or via molecular cloning of cDNA made from the mRNA. The sequence of the cloned cDNA can be determined using DNA sequencing techniques which are well known in the art. The cDNA can also be sequenced via the polymerase chain reaction (PCR).

Alternatively, mismatch detection can be used to detect point mutations in the p53 gene or its mRNA product. The method can involve the use of a labeled riboprobe which is complementary to the human wild-type p53 gene. The riboprobe and either mRNA or DNA isolated from the tumor tissue are annealed (hybridized) together and subsequently digested with the enzyme RNase A which is able to detect some mismatches in a duplex RNA structure. If a mismatch is detected by RNase A, it cleaves at the site of the mismatch. Thus, when the annealed RNA preparation is separated on an electrophoretic gel matrix, if a mismatch has been detected and cleaved by RNase A, an RNA product will be seen which is smaller than the full-length duplex RNA for the riboprobe and the p53 mRNA or DNA. The riboprobe need not be the full length of the p53 mRNA or gene but can be a segment of either. If the riboprobe comprises only a segment of the p53 mRNA or gene it will be desirable to use a number of these probes to screen the whole mRNA sequence for mismatches.

In similar fashion, DNA probes can be used to detect mismatches, through enzymatic or chemical cleavage. See, e.g., Cotton et al., Proc. Natl. Acad. Sci. USA, vol. 85, 4397, 1988; and Shenk et al., Proc. Natl. Acad. Sci. USA, vol. 72, p. 989, 1975. Alternatively, mismatches can be detected by shifts in the electrophoretic mobility of mismatched duplexes relative to matched duplexes. See, e.g., Cariello, Human Genetics, vol. 42, p. 726, 1988. With either riboprobes or DNA probes, the cellular mRNA or DNA which might contain a mutation can be amplified using PCR (see below) before hybridization.

DNA sequences of the p53 gene from the tumor tissue which have been amplified by use of polymerase chain reaction can also be screened using allele-specific probes. These probes are nucleic acid oligomers, each of which contains a region of the p53 gene sequence harboring a known mutation. For example, one oligomer can be about 30 nucleotides in length, corresponding to a portion of the p53 gene sequence. At the position coding for the 175th codon of p53 gene the oligomer encodes an alanine, rather than the wild-type codon valine. By use of a battery of such allele-specific probes, the PCR amplification products can be screened to identify the presence of a previously identified mutation in the p53 gene. Hybridization of allele-specific probes with amplified p53 sequences can be performed, for example, on a nylon filter. Hybridization to a particular probe indicates the presence of the same mutation in the tumor tissue as in the allele-specific probe.

The identification of p53 gene structural changes in tumor cells has been facilitated through the development and application of a diverse series of high resolution, high throughput microarray platforms. Essentially there are two types of array; those that carry PCR products from cloned nucleic acids {e.g. cDNA, BACs, cosmids) and those that use oligonucleotides. Each has advantages and disadvantages but it is now possible to survey genome wide DNA copy number abnormalities and expression levels to allow correlations between losses, gains and amplifications in tumor cells with genes that are over- and under-expressed in the same samples. The gene expression arrays that provide estimates of mRNA levels in tumors have given rise to exon-specific arrays that can identify both gene expression levels, alternative splicing events and mRNA processing alterations. Oligonucleotide arrays are also being used to interrogate single nucleotide polymorphisms (SNPs) throughout the genome for linkage and association studies and these have been adapted to quantify copy number abnormalities and loss of heterozygosity events. Ultimately DNA sequencing arrays will allow resequencing of chromosome regions and whole genomes.

SNP-based arrays or other gene arrays or chips are also contemplated to determine the presence of wild-type p53 allele and the structure of mutations. A single nucleotide polymorphism (SNP), a variation at a single site in DNA, is the most frequent type of variation in the genome. For example, there are an estimated 5-10 million SNPs in the human genome. As SNPs are highly conserved throughout evolution and within a population, the map of SNPs serves as an excellent genotypic marker for research. An SNP array is a useful tool to study the whole genome.

In addition, SNP array can be used for studying the Loss Of Heterozygosity (LOH). LOH is a form of allelic imbalance that can result from the complete loss of an allele or from an increase in copy number of one allele relative to the other. While other chip-based methods (e.g., comparative genomic hybridization can detect only genomic gains or deletions), SNP array has the additional advantage of detecting copy number neutral LOH due to uniparental disomy (UPD). In UPD, one allele or whole chromosome from one parent are missing leading to reduplication of the other parental allele (uni-parental=from one parent, disomy=duplicated). In a disease setting this occurrence can be pathologic when the wild-type allele (e.g., from the mother) is missing and instead two copies of the heterozygous allele (e.g., from the father) are present. This usage of SNP array has a huge potential in cancer diagnostics as LOH is a prominent characteristic of most human cancers. Recent studies based on the SNP array technology have shown that not only solid tumors (e.g. gastric cancer, liver cancer etc) but also hematologic malignancies (ALL, MDS, CML etc) have a high rate of LOH due to genomic deletions or UPD and genomic gains. In the present disclosure, using high density SNP array to detect LOH allows identification of pattern of allelic imbalance to determine the presence of wild-type p53 allele (Lips et ah, 2005; Lai et al, 2007).

Examples for current p53 gene sequence and single nucleotide polymorphism arrays include p53 Gene Chip (Affymetrix, Santa Clara, Calif.), Roche p53 Ampli-Chip (Roche Molecular Systems, Pleasanton, Calif.), GeneChip Mapping arrays (Affymetrix, Santa Clara, Calif.), SNP Array 6.0 (Affymetrix, Santa Clara, Calif.), BeadArrays (Illumina, San Diego, Calif.), etc.

Mutations of wild-type p53 genes can also be detected on the basis of the mutation of a wild-type expression product of the p53 gene. Such expression products include both the mRNA as well as the p53 protein product itself. Point mutations can be detected by sequencing the mRNA directly or via molecular cloning of cDNA made from the mRNA. The sequence of the cloned cDNA can be determined using DNA sequencing techniques which are well known in the art. The cDNA can also be sequenced via the polymerase chain reaction (PCR). A panel of monoclonal antibodies could be used in which each of the epitopes involved in p53 functions are represented by a monoclonal antibody. Loss or perturbation of binding of a monoclonal antibody in the panel would indicate mutational alteration of the p53 protein and thus of the p53 gene itself. Mutant p53 genes or gene products can also be detected in body samples, such as, serum, stool, or other body fluids, such as urine and sputum. The same techniques discussed above for detection of mutant p53 genes or gene products in tissues can be applied to other body samples. 2. Assessment of p53 Protein Level

Loss of wild-type p53 genes can also be detected by screening for loss of wild-type p53 protein function. Although all of the functions which the p53 protein undoubtedly possesses have yet to be elucidated, at least two specific functions are known. Protein p53 binds to the SV40 large T antigen as well as to the adenovirus E1B antigen. Loss of the ability of the p53 protein to bind to either or both of these antigens indicates a mutational alteration in the protein which reflects a mutational alteration of the gene itself. Alternatively, a panel of monoclonal antibodies could be used in which each of the epitopes involved in p53 functions are represented by a monoclonal antibody. Loss or perturbation of binding of a monoclonal antibody in the panel would indicate mutational alteration of the p53 protein and thus of the p53 gene itself. Any means for detecting an altered p53 protein can be used to detect loss of wild-type p53 genes.

Mutant p53 genes or gene products can also be detected in body samples, such as, serum, stool, or other body fluids, such as urine and sputum. The same techniques discussed above for detection of mutant p53 genes or gene products in tissues can be applied to other body samples.

Determination of the lack of p53 deactivating mutation and/or expression of wild type p53 in the subject with solid tumor can be performed any time before, during or after the administration of the peptidomimetic macrocycles. In some embodiments, the determination of the lack of a p53 deactivating mutation and/or expression of wild type p53 is performed before the first administration of the peptidomimetic macrocycle to the subject, for example about 5 years-1 month, 4 years-1 month, 3 years-1 month, 2 years-1 month, 1 years-1 month, 5 years-1 week, 4 years-1 week, 3 years-1 month, 2 years-1 week, 1 year-1 week, 5 years-1 day, 4 years-1 day, 3 years-1 days, 2 years-1 day, 1 year-1 day, 15 months-1 month, 15 months-1 week, 15 months-1 day, 12 months-1 month, 12 months-1 week, 12 months-1 day, 6 months-1 month, 6 months-1 week, 6 months-1 day, 3 months-1 month, 3 months-1 week, or 3 months-1 day prior to the first administration of the peptidomimetic macrocycle to the subject. In some examples, the confirmation of the lack of the p53 deactivating mutation and/or expression of wild type p53 is performed up to 6 years, 5 years, 4 years, 3 years, 24 months, 23 months, 22 months, 21 months, 20 months, 19 months, 18 months, 17 months, 16 months, 15 months, 14 months, 13 months, 12 months, 11 months, 10 months, 9 months, 8 months, 7 months, 6 months, 5 months, 4 months, 3 months, 2 months, 1 months, 4 weeks (28 days), 3 weeks (21 days), 2 weeks (14 days), 1 week (7 days), 6 days, 5 days, 4 days, 3 days, 2 days or 1 day before the first administration of the peptidomimetic macrocycle to the subject. In some examples the confirmation of the lack of the p53 deactivating mutation is performed within 1 month of the first administration of the peptidomimetic macrocycle to the subject. In some examples the confirmation of the lack of the p53 deactivating mutation is performed within 21 days of the first administration of the peptidomimetic macrocycle to the subject.

Solid Tumors

Solid tumors that can be treated by the instant methods include tumors and/or metastasis (wherever located) other than lymphatic cancer, for example brain and other central nervous system tumors (including but not limited to tumors of the meninges, brain, spinal cord, cranial nerves and other parts of central nervous system, e.g. glioblastomas or medulla blastomas); head and/or neck cancer; breast tumors; circulatory system tumors (including but not limited to heart, mediastinum and pleura, and other intrathoracic organs, vascular tumors and tumor-associated vascular tissue); excretory system tumors (including but not limited to tumors of kidney, renal pelvis, ureter, bladder, other and unspecified urinary organs); gastrointestinal tract tumors (including but not limited to tumors of oesophagus, stomach, small intestine, colon, colorectal, rectosigmoid junction, rectum, anus and anal canal, tumors involving the liver and intrahepatic bile ducts, gall bladder, other and unspecified parts of biliary tract, pancreas, other and digestive organs); oral cavity tumors (including but not limited to tumors of lip, tongue, gum, floor of mouth, palate, and other parts of mouth, parotid gland, and other parts of the salivary glands, tonsil, oropharynx, nasopharynx, pyriform sinus, hypopharynx, and other sites in the lip, oral cavity and pharynx); reproductive system tumors (including but not limited to tumors of vulva, vagina, Cervix uteri, Corpus uteri, uterus, ovary, and other sites associated with female genital organs, placenta, penis, prostate, testis, and other sites associated with male genital organs); respiratory tract tumors (including but not limited to tumors of nasal cavity and middle ear, accessory sinuses, larynx, trachea, bronchus and lung, e.g. small cell lung cancer or non-small cell lung cancer); skeletal system tumors (including but not limited to tumors of bone and articular cartilage of limbs, bone articular cartilage and other sites); skin tumors (including but not limited to malignant melanoma of the skin, non-melanoma skin cancer, basal cell carcinoma of skin, squamous cell carcinoma of skin, mesothelioma, Kaposi's sarcoma); and tumors involving other tissues including peripheral nerves and autonomic nervous system, connective and soft tissue, retroperitoneum and peritoneum, eye and adnexa, thyroid, adrenal gland and other endocrine glands and related structures, secondary and unspecified malignant neoplasm of lymph nodes, secondary malignant neoplasm of respiratory and digestive systems and secondary malignant neoplasm of other sites.

In some examples, the solid tumor treated by the methods of the instant disclosure is pancreatic cancer, bladder cancer, colon cancer, liver cancer, colorectal cancer (colon cancer or rectal cancer), breast cancer, prostate cancer, renal cancer, hepatocellular cancer, lung cancer, ovarian cancer, cervical cancer, gastric cancer, esophageal cancer, head and neck cancer, melanoma, neuroendocrine cancers, CNS cancers, brain tumors, bone cancer, skin cancer, ocular tumor, choriocarcinoma (tumor of the placenta), sarcoma or soft tissue cancer.

In some examples, the solid tumor to be treated by the methods of the instant disclosure is selected bladder cancer, bone cancer, breast cancer, cervical cancer, CNS cancer, colon cancer, ocular tumor, renal cancer, liver cancer, lung cancer, pancreatic cancer, choriocarcinoma (tumor of the placenta), prostate cancer, sarcoma, skin cancer, soft tissue cancer or gastric cancer.

In some examples, the solid tumor treated by the methods of the instant disclosure is breast cancer. Non limiting examples of breast cancer that can be treated by the instant methods include ductal carcinoma in situ (DCIS or intraductal carcinoma), lobular carcinoma in situ (LCIS), invasive (or infiltrating) ductal carcinoma, invasive (or infiltrating) lobular carcinoma, inflammatory breast cancer, triple-negative breast cancer, paget disease of the nipple, phyllodes tumor (phylloides tumor or cystosarcoma phyllodes), angiosarcoma, adenoid cystic (or adenocystic) carcinoma, low-grade adenosquamous carcinoma, medullary carcinoma, papillary carcinoma, tubular carcinoma, metaplastic carcinoma, micropapillary carcinoma, and mixed carcinoma.

In some examples, the solid tumor treated by the methods of the instant disclosure is bone cancer. Non limiting examples of bone cancer that can be treated by the instant methods include osteosarcoma, chondrosarcoma, the Ewing Sarcoma Family of Tumors (ESFTs).

In some examples, the solid tumor treated by the methods of the instant disclosure is skin cancer. Non limiting examples of skin cancer that can be treated by the instant methods include melanoma, basal cell skin cancer, and squamous cell skin cancer.

In some examples, the solid tumor treated by the methods of the instant disclosure is ocular tumor. Non limiting examples of ocular tumor that can be treated by the methods of the instant disclosure include ocular tumor is choroidal nevus, choroidal melanoma, choroidal metastasis, choroidal hemangioma, choroidal osteoma, iris melanoma, uveal melanoma, intraocular lymphoma, melanocytoma, metastasis retinal capillary hemangiomas, congenital hypertrophy of the RPE, RPE adenoma or retinoblastoma.

In some embodiments solid tumors treated by the methods disclosed herein exclude cancers that are known to be associated with HPV (Human papillomavirus). The excluded group includes HPV positive cervical cancer, HPV positive anal cancer, and HPV head and neck cancers, such as oropharyngeal cancers.

The effectiveness and/or response of cancer treatment by the methods disclosed herein can be determined by any method known in art. The response can be a complete response, and which can be an objective response, a clinical response, or a pathological response to treatment. For example, the response can be determined based upon the techniques for evaluating response to treatment of solid tumors as described in Therese et al., New Guidelines to Evaluate the Response to Treatment in Solid Tumors, J. of the National Cancer Institute 92(3):205-207 (2000), which is hereby incorporated by reference in its entirety. The response can be a duration of survival (or probability of such duration) or progression-free interval. The timing or duration of such events can be determined from about the time of diagnosis, or from about the time treatment is initiated or from about the time treatment is finished (like the final administration of the peptidomimetic macrocycle). Alternatively, the response can be based upon a reduction in tumor size, tumor volume, or tumor metabolism, or based upon overall tumor burden, or based upon levels of serum markers especially where elevated in the disease state.

The response in individual patients can be characterized as a complete response, a partial response, stable disease, and progressive disease, as these terms are understood in the art. In some embodiments, the response is complete response (CR). Complete response, in some examples can be defined as disappearance of all target lesions i.e. any pathological lymph nodes (whether target or non-target) must have reduction in short axis to <10 mm. In certain embodiments, the response is a partial response (PR). Partial response can be defined to mean at least 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. In some embodiments, the response is progressive disease (PD). Progressive disease can be defined as at least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest) and an absolute increase of at least 5 mm in the sum of diameters of target lesions. The appearance of one or more new lesions can also be considered as progression. In some embodiments, the disease can be stable disease (SD). Stable disease can be characterized by neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, taking as reference the smallest sum diameters while on study. In certain embodiments, the response is a pathological complete response. A pathological complete response, e.g., as determined by a pathologist following examination of tissue removed at the time of surgery or biopsy, generally refers to an absence of histological evidence of invasive tumor cells in the surgical specimen.

Combination Treatment

Also provided herein are combination therapies for the treatment of a solid tumor which involve the administration of the peptidomimetic macrocycles disclosed herein in combination with one or more additional therapies to a subject with solid tumor determined to lack a p53 deactivating mutation and/or express wild type p53. In a specific embodiment, presented herein are combination therapies for the treatment of solid tumor which involve the administration of an effective amount of the peptidomimetic macrocycles in combination with an effective amount of another therapy to a subject with a solid tumor determined to lack a p53 deactivating mutation and/or with a solid tumor expressing wild type p53.

As used herein, the term “in combination,” refers, in the context of the administration of the peptidomimetic macrocycles, to the administration of the peptidomimetic macrocycles prior to, concurrently with, or subsequent to the administration of one or more additional therapies (e.g., agents, surgery, or radiation) for use in treating solid tumor. The use of the term “in combination” does not restrict the order in which the peptidomimetic macrocycles and one or more additional therapies are administered to a subject. In specific embodiments, the interval of time between the administration of the peptidomimetic macrocycles and the administration of one or more additional therapies can be about 1-5 minutes, 1-30 minutes, 30 minutes to 60 minutes, 1 hour, 1-2 hours, 2-6 hours, 2-12 hours, 12-24 hours, 1-2 days, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 1 week, 2 weeks, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 7 weeks, 8 weeks, 9 weeks, 10 weeks, 15 weeks, 20 weeks, 26 weeks, 52 weeks, 11-15 weeks, 15-20 weeks, 20-30 weeks, 30-40 weeks, 40-50 weeks, 1 month, 2 months, 3 months, 4 months 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, 1 year, 2 years, or any period of time in between. In certain embodiments, the peptidomimetic macrocycles and one or more additional therapies are administered less than 1 day, 1 week, 2 weeks, 3 weeks, 4 weeks, one month, 2 months, 3 months, 6 months, 1 year, 2 years, or 5 years apart.

In some embodiments, the combination therapies provided herein involve administering of the peptidomimetic macrocycles 1-2 times a week, once every week, once every 2 weeks, once every 3 weeks, once every 4 weeks, once every 5 weeks, once every 6 weeks, once every 7 weeks or once every 8 weeks and administering one or more additional therapies once a week, once every 2 weeks, once every 3 weeks, once every 4 weeks, once every month, once every 2 months (e.g., approximately 8 weeks), once every 3 months (e.g., approximately 12 weeks), or once every 4 months (e.g., approximately 16 weeks). In certain embodiments, the peptidomimetic macrocycles and one or more additional therapies are cyclically administered to a subject. Cycling therapy involves the administration of the peptidomimetic macrocycles compounds for a period of time, followed by the administration of one or more additional therapies for a period of time, and repeating this sequential administration. In certain embodiments, cycling therapy can also include a period of rest where the peptidomimetic macrocycles or the additional therapy is not administered for a period of time (e.g., 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 1 week, 2 weeks, 3 weeks, 4 weeks, 5 weeks, 10 weeks, 20 weeks, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, 2 years, or 3 years). In an embodiment, the number of cycles administered is from 1 to 12 cycles, from 2 to 10 cycles, or from 2 to 8 cycles.

In some embodiments, the methods for treating solid tumor provided herein comprise administering the peptidomimetic macrocycles as a single agent for a period of time prior to administering the peptidomimetic macrocycles in combination with an additional therapy. In certain embodiments, the methods for treating cancer provided herein comprise administering an additional therapy alone for a period of time prior to administering the peptidomimetic macrocycles in combination with the additional therapy.

In some embodiments, the administration of the peptidomimetic macrocycles and one or more additional therapies in accordance with the methods presented herein have an additive effect relative the administration of the peptidomimetic macrocycles or said one or more additional therapies alone. In some embodiments, the administration of the peptidomimetic macrocycles and one or more additional therapies in accordance with the methods presented herein have a synergistic effect relative to the administration of the peptidomimetic macrocycles or said one or more additional therapies alone.

As used herein, the term “synergistic,” refers to the effect of the administration of the peptidomimetic macrocycles in combination with one or more additional therapies (e.g., agents), which combination is more effective than the additive effects of any two or more single therapies (e.g., agents). In a specific embodiment, a synergistic effect of a combination therapy permits the use of lower dosages (e.g., sub-optimal doses) of the peptidomimetic macrocycles or an additional therapy and/or less frequent administration of the peptidomimetic macrocycles or an additional therapy to a subject. In certain embodiments, the ability to utilize lower dosages of the peptidomimetic macrocycles or of an additional therapy and/or to administer the peptidomimetic macrocycles or said additional therapy less frequently reduces the toxicity associated with the administration of the peptidomimetic macrocycles or of said additional therapy, respectively, to a subject without reducing the efficacy of the peptidomimetic macrocycles or of said additional therapy, respectively, in the treatment of solid tumor. In some embodiments, a synergistic effect results in improved efficacy of the peptidomimetic macrocycles and each of said additional therapies in treating cancer. In some embodiments, a synergistic effect of a combination of the peptidomimetic macrocycles and one or more additional therapies avoids or reduces adverse or unwanted side effects associated with the use of any single therapy.

The combination of the peptidomimetic macrocycles and one or more additional therapies can be administered to a subject in the same pharmaceutical composition. Alternatively, the peptidomimetic macrocycles and one or more additional therapies can be administered concurrently to a subject in separate pharmaceutical compositions. The peptidomimetic macrocycles and one or more additional therapies can be administered sequentially to a subject in separate pharmaceutical compositions. The peptidomimetic macrocycles compounds and one or more additional therapies can also be administered to a subject by the same or different routes of administration.

The combination therapies provided herein involve administering to a subject to in need thereof the peptidomimetic macrocycles in combination with conventional, or known, therapies for treating cancer. Other therapies for cancer or a condition associated therewith are aimed at controlling or relieving one or more symptoms. Accordingly, in some embodiments, the combination therapies provided herein involve administering to a subject to in need thereof a pain reliever, or other therapies aimed at alleviating or controlling one or more symptoms associated with or a condition associated therewith.

Non-limiting specific examples of anti-cancer agents that can be used in combination with the peptidomimetic macrocycles include: a hormonal agent (e.g., aromatase inhibitor, selective estrogen receptor modulator (SERM), and estrogen receptor antagonist), chemotherapeutic agent (e.g., microtubule disassembly blocker, antimetabolite, topoisomerase inhibitor, and DNA crosslinker or damaging agent), anti-antigenic agent (e.g., VEGF antagonist, receptor antagonist, integrin antagonist, vascular targeting agent (VTA)/vascular disrupting agent (VDA)), radiation therapy, and conventional surgery.

Non-limiting examples of hormonal agents that can be used in combination with the peptidomimetic macrocycles include aromatase inhibitors, SERMs, and estrogen receptor antagonists. Hormonal agents that are aromatase inhibitors can be steroidal or no steroidal. Non-limiting examples of no steroidal hormonal agents include letrozole, anastrozole, aminoglutethimide, fadrozole, and vorozole. Non-limiting examples of steroidal hormonal agents include aromasin (exemestane), formestane, and testolactone. Non-limiting examples of hormonal agents that are SERMs include tamoxifen (branded/marketed as Nolvadex®), afimoxifene, arzoxifene, bazedoxifene, clomifene, femarelle, lasofoxifene, ormeloxifene, raloxifene, and toremifene. Non-limiting examples of hormonal agents that are estrogen receptor antagonists include fulvestrant. Other hormonal agents include but are not limited to abiraterone and lonaprisan.

Non-limiting examples of chemotherapeutic agents that can be used in combination with of peptidomimetic macrocycles include microtubule disassembly blocker, antimetabolite, topoisomerase inhibitor, and DNA crosslinker or damaging agent. Chemotherapeutic agents that are microtubule disassembly blockers include, but are not limited to, taxanes (e.g., paclitaxel (branded/marketed as TAXOL®), docetaxel, abraxane, larotaxel, ortataxel, and tesetaxel); epothilones (e.g., ixabepilone); and vinca alkaloids (e.g., vinorelbine, vinblastine, vindesine, and vincristine (branded/marketed as ONCOVIN®)).

Chemotherapeutic agents that are antimetabolites include, but are not limited to, folate anitmetabolites (e.g., methotrexate, aminopterin, pemetrexed, raltitrexed); purine antimetabolites (e.g., cladribine, clofarabine, fludarabine, mercaptopurine, pentostatin, thioguanine); pyrimidine antimetabolites (e.g., 5-fluorouracil, capcitabine, gemcitabine (GEMZAR®), cytarabine, decitabine, floxuridine, tegafur); and deoxyribonucleotide antimetabolites (e.g., hydroxyurea).

Chemotherapeutic agents that are topoisomerase inhibitors include, but are not limited to, class I (camptotheca) topoisomerase inhibitors (e.g., topotecan (branded/marketed as HYCAMTIN®) irinotecan, rubitecan, and belotecan); class II (podophyllum) topoisomerase inhibitors (e.g., etoposide or VP-16, and teniposide); anthracyclines (e.g., doxorubicin, epirubicin, Doxil, aclarubicin, amrubicin, daunorubicin, idarubicin, pirarubicin, valrubicin, and zorubicin); and anthracenediones (e.g., mitoxantrone, and pixantrone).

Chemotherapeutic agents that are DNA crosslinkers (or DNA damaging agents) include, but are not limited to, alkylating agents (e.g., cyclophosphamide, mechlorethamine, ifosfamide (branded/marketed as IFEX®), trofosfamide, chlorambucil, melphalan, prednimustine, bendamustine, uramustine, estramustine, carmustine (branded/marketed as BiCNU®), lomustine, semustine, fotemustine, nimustine, ranimustine, streptozocin, busulfan, mannosulfan, treosulfan, carboquone, N,N′N′-triethylenethiophosphoramide, triaziquone, triethylenemelamine); alkylating-like agents (e.g., carboplatin (branded/marketed as PARAPLATIN®), cisplatin, oxaliplatin, nedaplatin, triplatin tetranitrate, satraplatin, picoplatin); nonclassical DNA crosslinkers (e.g., procarbazine, dacarbazine, temozolomide (branded/marketed as TEMODAR®), altretamine, mitobronitol); and intercalating agents (e.g., actinomycin, bleomycin, mitomycin, and plicamycin).

Non-limiting examples of other therapies that can be administered to a subject in combination with the peptidomimetic macrocycles include: (1) a statin such as lovastatin (e.g., branded/marketed as MEVACOR®); (2) an mTOR inhibitor such as sirolimus which is also known as Rapamycin (e.g., branded/marketed as RAPAMUNE®), temsirolimus (e.g., branded/marketed as TORISEL®), evorolimus (e.g., branded/marketed as AFINITOR®), and deforolimus; (3) a farnesyltransferase inhibitor agent such as tipifarnib; (4) an antifibrotic agent such as pirfenidone; (5) a pegylated interferon such as PEG-interferon alfa-2b; (6) a CNS stimulant such as methylphenidate (branded/marketed as RITALIN®); (7) a HER-2 antagonist such as anti-HER-2 antibody (e.g., trastuzumab) and kinase inhibitor (e.g., lapatinib); (8) an IGF-1 antagonist such as an anti-IGF-1 antibody (e.g., AVE1642 and IMC-A11) or an IGF-1 kinase inhibitor; (9) EGFR/HER-1 antagonist such as an anti-EGFR antibody (e.g., cetuximab, panitumamab) or EGFR kinase inhibitor (e.g., erlotinib; gefitinib); (10) SRC antagonist such as bosutinib; (11) cyclin dependent kinase (CDK) inhibitor such as seliciclib; (12) Janus kinase 2 inhibitor such as lestaurtinib; (13) proteasome inhibitor such as bortezomib; (14) phosphodiesterase inhibitor such as anagrelide; (15) inosine monophosphate dehydrogenase inhibitor such as tiazofurine; (16) lipoxygenase inhibitor such as masoprocol; (17) endothelin antagonist; (18) retinoid receptor antagonist such as tretinoin or alitretinoin; (19) immune modulator such as lenalidomide, pomalidomide, or thalidomide; (20) kinase (e.g., tyrosine kinase) inhibitor such as imatinib, dasatinib, erlotinib, nilotinib, gefitinib, sorafenib, sunitinib, lapatinib, or TG100801; (21) non-steroidal anti-inflammatory agent such as celecoxib (branded/marketed as CELEBREX®); (22) human granulocyte colony-stimulating factor (G-CSF) such as filgrastim (branded/marketed as NEUPOGEN®); (23) folinic acid or leucovorin calcium; (24) integrin antagonist such as an integrin α5β1-antagonist (e.g., JSM6427); (25) nuclear factor kappa beta (NF-κβ) antagonist such as OT-551, which is also an anti-oxidant. (26) hedgehog inhibitor such as CUR61414, cyclopamine, GDC-0449, and anti-hedgehog antibody; (27) histone deacetylase (HDAC) inhibitor such as SAHA (also known as vorinostat (branded/marketed as ZOLINZA)), PCI-24781, SB939, CHR-3996, CRA-024781, ITF2357, JNJ-26481585, or PCI-24781; (28) retinoid such as isotretinoin (e.g., branded/marketed as ACCUTANE®); (29) hepatocyte growth factor/scatter factor (HGF/SF) antagonist such as HGF/SF monoclonal antibody (e.g., AMG 102); (30) synthetic chemical such as antineoplaston; (31) anti-diabetic such as rosaiglitazone (e.g., branded/marketed as AVANDIA®); (32) antimalarial and amebicidal drug such as chloroquine (e.g., branded/marketed as ARALEN®); (33) synthetic bradykinin such as RMP-7; (34) platelet-derived growth factor receptor inhibitor such as SU-101; (35) receptor tyrosine kinase inhibitorsof Flk-1/KDR/VEGFR2, FGFR1 and PDGFR beta such as SU5416 and SU6668; (36) anti-inflammatory agent such as sulfasalazine (e.g., branded/marketed as AZULFIDINE®); and (37) TGF-beta antisense therapy.

In some embodiments a peptidomimetic macrocycles disclosed herein can inhibit one or more transporter enzymes (e.g., OATP1B1, OATP1B3, BSEP) at concentrations that can be clinically relevant. Therefore such a peptidomimetic macrocycles disclosed herein can interact with medications that are predominantly cleared by hepatobiliary transporters. In particular, methotrexate and statins (e.g., atorvastatin, fluvastatin lovastatin, pitavastatin pravastatin, rosuvastatin and simvastatin) may not be dosed within 48 h, 36 h, 24 h, or 12 h ((for example within 24 h) of the administration of such a peptidomimetic macrocycle. Exemplary medications that can be affected by co-administration of such a peptidomimetic macrocycles are listed below. In various embodiments one or more of the medications selected from Table 2 may not be dosed within 48 h, 36 h, 24 h, or 12 h (for example within 24 h) of the administration of such a peptidomimetic macrocycle.

TABLE 2 Exemplary medications that can be affected by co-administration with a peptidomimetic macrocycles disclosed herein. Medication Therapeutic Area Irinotecan Oncology Bosentan Pulmonary artery hypertension Caspofungin Antifungal Methotrexate Oncology & rheumatology Repaglinide Diabetes mellitus Atorvastatin Hypercholesterolemia Cerivastatin Hypercholesterolemia Fluvastatin Hypercholesterolemia Lovastatin Hypercholesterolemia Pitavastatin Hypercholesterolemia Pravastatin Hypercholesterolemia Rosuvastatin Hypercholesterolemia Simvastatin Hypercholesterolemia

EXAMPLES Example 1 Peptidomimetic Macrocycles

Peptidomimetic macrocycles were synthesized, purified and analyzed as previously described and as described below (Schafmeister et al., J. Am. Chem. Soc. 122:5891-5892 (2000); Schafineister & Verdine, J. Am. Chem. Soc. 122:5891 (2005); Walensky et al., Science 305:1466-1470 (2004); and U.S. Pat. No. 7,192,713). Peptidomimetic macrocycles were designed by replacing two or more naturally occurring amino acids with the corresponding synthetic amino acids. Substitutions were made at i and i+4, and i and i+7 positions. Peptide synthesis was performed either manually or on an automated peptide synthesizer (Applied Biosystems, model 433A), using solid phase conditions, rink amide AM resin (Novabiochem), and Fmoc main-chain protecting group chemistry. For the coupling of natural Fmoc-protected amino acids (Novabiochem), 10 equivalents of amino acid and a 1:1:2 molar ratio of coupling reagents HBTU/HOBt (Novabiochem)/DIEA were employed. Non-natural amino acids (4 equiv) were coupled with a 1:1:2 molar ratio of HATU (Applied Biosystems)/HOBt/DIEA. The N-termini of the synthetic peptides were acetylated, while the C-termini were amidated.

Purification of cross-linked compounds was achieved by high performance liquid chromatography (HPLC) (Varian ProStar) on a reverse phase C18 column (Varian) to yield the pure compounds. Chemical composition of the pure products was confirmed by LC/MS mass spectrometry (Micromass LCT interfaced with Agilent 1100 HPLC system) and amino acid analysis (Applied Biosystems, model 420A).

The following protocol was used in the synthesis of dialkyne-crosslinked peptidomimetic macrocycles, including SP662, SP663 and SP664. Fully protected resin-bound peptides were synthesized on a PEG-PS resin (loading 0.45 mmol/g) on a 0.2 mmol scale. Deprotection of the temporary Fmoc group was achieved by 3×10 min treatments of the resin bound peptide with 20% (v/v) piperidine in DMF. After washing with NMP (3×), dichloromethane (3×) and NMP (3×), coupling of each successive amino acid was achieved with 1×60 min incubation with the appropriate preactivated Fmoc-amino acid derivative. All protected amino acids (0.4 mmol) were dissolved in NMP and activated with HCTU (0.4 mmol) and DIEA (0.8 mmol) prior to transfer of the coupling solution to the deprotected resin-bound peptide. After coupling was completed, the resin was washed in preparation for the next deprotection/coupling cycle. Acetylation of the amino terminus was carried out in the presence of acetic anhydride/DIEA in NMP. The LC-MS analysis of a cleaved and deprotected sample obtained from an aliquot of the fully assembled resin-bound peptide was accomplished in order to verifying the completion of each coupling. In a typical example, tetrahydrofuran (4 ml) and triethylamine (2 ml) were added to the peptide resin (0.2 mmol) in a 40 ml glass vial and shaken for 10 minutes. Pd(PPh₃)₂Cl₂ (0.014 g, 0.02 mmol) and copper iodide (0.008 g, 0.04 mmol) were then added and the resulting reaction mixture was mechanically shaken 16 hours while open to atmosphere. The diyne-cyclized resin-bound peptides were deprotected and cleaved from the solid support by treatment with TFA/H₂O/TIS (95/5/5 v/v) for 2.5 h at room temperature. After filtration of the resin the TFA solution was precipitated in cold diethyl ether and centrifuged to yield the desired product as a solid. The crude product was purified by preparative HPLC.

The following protocol was used in the synthesis of single alkyne-crosslinked peptidomimetic macrocycles, including SP665. Fully protected resin-bound peptides were synthesized on a Rink amide MBHA resin (loading 0.62 mmol/g) on a 0.1 mmol scale. Deprotection of the temporary Fmoc group was achieved by 2×20 min treatments of the resin bound peptide with 25% (v/v) piperidine in NMP. After extensive flow washing with NMP and dichloromethane, coupling of each successive amino acid was achieved with 1×60 min incubation with the appropriate preactivated Fmoc-amino acid derivative. All protected amino acids (1 mmol) were dissolved in NMP and activated with HCTU (1 mmol) and DIEA (1 mmol) prior to transfer of the coupling solution to the deprotected resin-bound peptide. After coupling was completed, the resin was extensively flow washed in preparation for the next deprotection/coupling cycle. Acetylation of the amino terminus was carried out in the presence of acetic anhydride/DIEA in NMP/NMM. The LC-MS analysis of a cleaved and deprotected sample obtained from an aliquot of the fully assembled resin-bound peptide was accomplished in order to verifying the completion of each coupling. In a typical example, the peptide resin (0.1 mmol) was washed with DCM. Resin was loaded into a microwave vial. The vessel was evacuated and purged with nitrogen. Molybdenumhexacarbonyl (0.01 eq, Sigma Aldrich 199959) was added. Anhydrous chlorobenzene was added to the reaction vessel. Then 2-fluorophenol (1 eq, Sigma Aldrich F12804) was added. The reaction was then loaded into the microwave and held at 130° C. for 10 minutes. Reaction may need to be pushed a subsequent time for completion. The alkyne metathesized resin-bound peptides were deprotected and cleaved from the solid support by treatment with TFA/H₂O/TIS (94/3/3 v/v) for 3 h at room temperature. After filtration of the resin the TFA solution was precipitated in cold diethyl ether and centrifuged to yield the desired product as a solid. The crude product was purified by preparative HPLC.

Table 3 shows a list of peptidomimetic macrocycles prepared.

TABLE 3 SEQ Calc Calc Calc ID Exact Found (M + (M + (M + Sequence NO: Isomer Mass Mass 1)/1 2)/2 3)/3   1 Ac-F$r8AYWEAc3cL$AAA-NH₂  10 1456.78 729.44 1457.79 729.4 486.6   2 Ac-F$r8AYWEAc3cL$AAibA-NH₂  11 1470.79 736.4 1471.8 736.4 491.27   3 Ac-LTF$r8AYWAQL$SANle-NH₂  12 1715.97 859.02 1716.98 858.99 573   4 Ac-LTF$r8AYWAQL$SAL-NH₂  13 1715.97 859.02 1716.98 858.99 573   5 Ac-LTF$r8AyWAQL$SAM-NH₂  14 1733.92 868.48 1734.93 867.97 578.98   6 Ac-LTF$r8AYWAQL$SAhL-NH₂  15 1729.98 865.98 1730.99 866 577.67   7 Ac-LTF$r8AYWAQL$SAF-NH₂  16 1749.95 876.36 1750.96 875.98 584.32   8 Ac-LTF$r8AYWAQL$SAI-NH₂  17 1715.97 859.02 1716.98 858.99 573   9 Ac-LTF$r8AYWAQL$SAChg-NH₂  18 1741.98 871.98 1742.99 872 581.67  10 Ac-LTF$r8AYWAQL$SAAib-NH₂  19 1687.93 845.36 1688.94 844.97 563.65  11 Ac-LTF$r8AYWAQL$SAA-NH₂  20 1673.92 838.01 1674.93 837.97 558.98  12 Ac-LTF$r8AYWA$L$S$Nle-NH₂  21 1767.04 884.77 1768.05 884.53 590.02  13 Ac-LTF$r8AYWA$L$S$A-NH₂  22 1724.99 864.23 1726 863.5 576  14 Ac-F$r8AYWEAc3cL$AANle-NH₂  23 1498.82 750.46 1499.83 750.42 500.61  15 Ac-F$r8AYWEAc3cL$AAL-NH₂  24 1498.82 750.46 1499.83 750.42 500.61  16 Ac-F$r8AYWEAc3cL$AAM-NH₂  25 1516.78 759.41 1517.79 759.4 506.6  17 Ac-F$r8AYWEAc3cL$AAhL-NH₂  26 1512.84 757.49 1513.85 757.43 505.29  18 Ac-F$r8AYWEAc3cL$AAF-NH₂  27 1532.81 767.48 1533.82 767.41 511.94  19 Ac-F$r8AYWEAc3cL$AAI-NH₂  28 1498.82 750.39 1499.83 750.42 500.61  20 Ac-F$r8AYWEAc3cL$AAChg-NH₂  29 1524.84 763.48 1525.85 763.43 509.29  21 Ac-F$r8AYWEAc3cL$AACha-NH₂  30 1538.85 770.44 1539.86 770.43 513.96  22 Ac-F$r8AYWEAc3cL$AAAib-NH₂  31 1470.79 736.84 1471.8 736.4 491.27  23 Ac-LTF$r8AYWAQL$AAAibV-NH₂  32 1771.01 885.81 1772.02 886.51 591.34  24 Ac-LTF$r8AYWAQL$AAAibV-NH₂  33 iso2 1771.01 886.26 1772.02 886.51 591.34  25 Ac-LTF$r8AYWAQL$SAibAA-NH₂  34 1758.97 879.89 1759.98 880.49 587.33  26 Ac-LTF$r8AYWAQL$SAibAA-NH₂  35 iso2 1758.97 880.34 1759.98 880.49 587.33  27 Ac-HLTF$r8HHWHQL$AANleNle-NH₂  36 2056.15 1028.86 2057.16 1029.08 686.39  28 Ac-DLTF$r8HHWHQL$RRLV-NH₂  37 2190.23 731.15 2191.24 1096.12 731.08  29 Ac-HHTF$r8HHWHQL$AAML-NH₂  38 2098.08 700.43 2099.09 1050.05 700.37  30 Ac-F$r8HHWHQL$RRDCha-NH₂  39 1917.06 959.96 1918.07 959.54 640.03  31 Ac-F$r8HHWHQL$HRFV-NH₂  40 1876.02 938.65 1877.03 939.02 626.35  32 Ac-HLTF$r8HHWHQL$AAhLA-NH₂  41 2028.12 677.2 2029.13 1015.07 677.05  33 Ac-DLTF$r8HHWHQL$RRChgl-NH₂  42 2230.26 1115.89 2231.27 1116.14 744.43  34 Ac-DLTF$r8HHWHQL$RRChgl-NH₂  43 iso2 2230.26 1115.96 2231.27 1116.14 744.43  35 Ac-HHTF$r8HHWHQL$AAChav-NH₂  44 2106.14 1053.95 2107.15 1054.08 703.05  36 Ac-F$r8HHWHQL$RRDa-NH₂  45 1834.99 918.3 1836 918.5 612.67  37 Ac-F$r8HHWHQL$HRAibG-NH₂  46 1771.95 886.77 1772.96 886.98 591.66  38 Ac-F$r8AYWAQL$HHNleL-NH₂  47 1730.97 866.57 1731.98 866.49 578  39 Ac-F$r8AYWSAL$HQANle-NH₂  48 1638.89 820.54 1639.9 820.45 547.3  40 Ac-F$r8AYWVQL$QHChgl-NH₂  49 1776.01 889.44 1777.02 889.01 593.01  41 Ac-F$r8AYWTAL$QQNlev-NH₂  50 1671.94 836.97 1672.95 836.98 558.32  42 Ac-F$r8AYWYQL$HAibAa-NH₂  51 1686.89 844.52 1687.9 844.45 563.3  43 Ac-LTF$r8AYWAQL$HHLa-NH₂  52 1903.05 952.27 1904.06 952.53 635.36  44 Ac-LTF$r8AYWAQL$HHLa-NH₂  53 iso2 1903.05 952.27 1904.06 952.53 635.36  45 Ac-LTF$r8AYWAQL$HQNlev-NH₂  54 1922.08 962.48 1923.09 962.05 641.7  46 Ac-LTF$r8AYWAQL$HQNlev-NH₂  55 iso2 1922.08 962.4 1923.09 962.05 641.7  47 Ac-LTF$r8AYWAQL$QQMl-NH₂  56 1945.05 973.95 1946.06 973.53 649.36  48 Ac-LTF$r8AYWAQL$QQMl-NH₂  57 iso2 1945.05 973.88 1946.06 973.53 649.36  49 Ac-LTF$r8AYWAQL$HAibhLV-NH₂  58 1893.09 948.31 1894.1 947.55 632.04  50 Ac-LTF$r8AYWAQL$AHFA-NH₂  59 1871.01 937.4 1872.02 936.51 624.68  51 Ac-HLTF$r8HHWHQL$AANle1-NH₂  60 2056.15 1028.79 2057.16 1029.08 686.39  52 Ac-DLTF$r8HHWHQL$RRLa-NH₂  61 2162.2 721.82 2163.21 1082.11 721.74  53 Ac-HHTF$r8HHWHQL$AAMv-NH₂  62 2084.07 1042.92 2085.08 1043.04 695.7  54 Ac-F$r8HHWHQL$RRDA-NH₂  63 1834.99 612.74 1836 918.5 612.67  55 Ac-F$r8HHWHQL$HRFCha-NH₂  64 1930.06 966.47 1931.07 966.04 644.36  56 Ac-F$r8AYWEAL$AA-NHAm  65 1443.82 1445.71 1444.83 722.92 482.28  57 Ac-F$r8AYWEAL$AA-NHiAm  66 1443.82 723.13 1444.83 722.92 482.28  58 Ac-F$r8AYWEAL$AA-NHnPr3Ph  67 1491.82 747.3 1492.83 746.92 498.28  59 Ac-F$r8AYWEAL$AA-NHnBu33Me  68 1457.83 1458.94 1458.84 729.92 486.95  60 Ac-F$r8AYWEAL$AA-NHPr  69 1415.79 709.28 1416.8 708.9 472.94  61 Ac-F$r8AYWEAL$AA-NHnEt2Ch  70 1483.85 1485.77 1484.86 742.93 495.62  62 Ac-F$r8AYWEAL$AA-NHnEt2Cp  71 1469.83 1470.78 1470.84 735.92 490.95  63 Ac-F$r8AYWEAL$AA-NHHex  72 1457.83 730.19 1458.84 729.92 486.95  64 Ac-LTF$r8AYWAQL$AAIA-NH₂  73 1771.01 885.81 1772.02 886.51 591.34  65 Ac-LTF$r8AYWAQL$AAIA-NH₂  74 iso2 1771.01 866.8 1772.02 886.51 591.34  66 Ac-LTF$r8AYWAAL$AAMA-NH₂  75 1731.94 867.08 1732.95 866.98 578.32  67 Ac-LTF$r8AYWAAL$AAMA-NH₂  76 iso2 1731.94 867.28 1732.95 866.98 578.32  68 Ac-LTF$r8AYWAQLSAANleA-NH₂  77 1771.01 867.1 1772.02 886.51 591.34  69 Ac-LTF$r8AYWAQL$AANleA-NH₂  78 iso2 1771.01 886.89 1772.02 886.51 591.34  70 Ac-LTF$r8AYWAQL$AAIa-NH₂  79 1771.01 886.8 1772.02 886.51 591.34  71 Ac-LTF$r8AYWAQL$AAIa-NH₂  80 iso2 1771.01 887.09 1772.02 886.51 591.34  72 Ac-LTF$r8AYWAAL$AAMa-NH₂  81 1731.94 867.17 1732.95 866.98 578.32  73 Ac-LTF$r8AYWAAL$AAMa-NH₂  82 iso2 1731.94 867.37 1732.95 866.98 578.32  74 Ac-LTF$r8AYWAQL$AANlea-NH₂  83 1771.01 887.08 1772.02 886.51 591.34  75 Ac-LTF$r8AYWAQL$AANlea-NH₂  84 iso2 1771.01 887.08 1772.02 886.51 591.34  76 Ac-LTF$r8AYWAAL$AAIv-NH₂  85 1742.02 872.37 1743.03 872.02 581.68  77 Ac-LTF$r8AYWAAL$AAIv-NH₂  86 iso2 1742.02 872.74 1743.03 872.02 581.68  78 Ac-LTF$r8AYWAQL$AAMv-NH₂  87 1817 910.02 1818.01 909.51 606.67  79 Ac-LTF$r8AYWAAL$AANlev-NH₂  88 1742.02 872.37 1743.03 872.02 581.68  80 Ac-LTF$r8AYWAAL$AANlev-NH₂  89 iso2 1742.02 872.28 1743.03 872.02 581.68  81 Ac-LTF$r8AYWAQL$AAIl-NH₂  90 1813.05 907.81 1814.06 907.53 605.36  82 Ac-LTF$r8AYWAQL$AAIl-NH₂  91 iso2 1813.05 907.81 1814.06 907.53 605.36  83 Ac-LTF$r8AYWAAL$AAM1-NH₂  92 1773.99 887.37 1775 888 592.34  84 Ac-LTF$r8AYWAQL$AANle1-NH₂  93 1813.05 907.61 1814.06 907.53 605.36  85 Ac-LTF$r8AYWAQL$AANle1-NH₂  94 iso2 1813.05 907.71 1814.06 907.53 605.36  86 Ac-F$r8AYWEAL$AAMA-NH₂  95 1575.82 789.02 1576.83 788.92 526.28  87 Ac-F$r8AYWEAL$AANleA-NH₂  96 1557.86 780.14 1558.87 779.94 520.29  88 Ac-F$r8AYWEAL$AAIa-NH₂  97 1557.86 780.33 1558.87 779.94 520.29  89 Ac-F$r8AYWEAL$AAMa-NH₂  98 1575.82 789.3 1576.83 788.92 526.28  90 Ac-F$r8AYWEAL$AANlea-NH₂  99 1557.86 779.4 1558.87 779.94 520.29  91 Ac-F$r8AYWEAL$AAIv-NH₂ 100 1585.89 794.29 1586.9 793.95 529.64  92 Ac-F$r8AYWEAL$AAMv-NH₂ 101 1603.85 803.08 1604.86 802.93 535.62  93 Ac-F$r8AYWEAL$AANlev-NH₂ 102 1585.89 793.46 1586.9 793.95 529.64  94 Ac-F$r8AYWEAL$AAI1-NH₂ 103 1599.91 800.49 1600.92 800.96 534.31  95 Ac-F$r8AYWEAL$AAM1-NH₂ 104 1617.86 809.44 1618.87 809.94 540.29  96 Ac-F$r8AYWEAL$AANle1-NH₂ 105 1599.91 801.7 1600.92 800.96 534.31  97 Ac-F$r8AYWEAL$AANle1-NH₂ 106 iso2 1599.91 801.42 1600.92 800.96 534.31  98 Ac-LTF$r8AY6c1WAQL$SAA-NH₂ 107 1707.88 855.72 1708.89 854.95 570.3  99 Ac-LTF$r8AY6c1WAQL$SAA-NH₂ 108 iso2 1707.88 855.35 1708.89 854.95 570.3 100 Ac-WTF$r8FYWSQL$AVAa-NH₂ 109 1922.01 962.21 1923.02 962.01 641.68 101 Ac-WTF$r8FYWSQL$AVAa-NH₂ 110 iso2 1922.01 962.49 1923.02 962.01 641.68 102 Ac-WTF$r8VYWSQL$AVA-NH₂ 111 1802.98 902.72 1803.99 902.5 602 103 Ac-WTF$r8VYWSQL$AVA-NH₂ 112 iso2 1802.98 903 1803.99 902.5 602 104 Ac-WTF$r8FYWSQL$SAAa-NH₂ 113 1909.98 956.47 1910.99 956 637.67 105 Ac-WTF$r8FYWSQL$SAAa-NH₂ 114 iso2 1909.98 956.47 1910.99 956 637.67 106 Ac-WTF$r8VYWSQL$AVAaa-NH₂ 115 1945.05 974.15 1946.06 973.53 649.36 107 Ac-WTF$r8VYWSQL$AVAaa-NH₂ 116 iso2 1945.05 973.78 1946.06 973.53 649.36 108 Ac-LTF$r8AYWAQL$AVG-NH₂ 117 1671.94 837.52 1672.95 836.98 558.32 109 Ac-LTF$r8AYWAQL$AVG-NH₂ 118 iso2 1671.94 837.21 1672.95 836.98 558.32 110 Ac-LTF$r8AYWAQL$AVQ-NH₂ 119 1742.98 872.74 1743.99 872.5 582 111 Ac-LTF$r8AYWAQL$AVQ-NH₂ 120 iso2 1742.98 872.74 1743.99 872.5 582 112 Ac-LTF$r8AYWAQL$SAa-NH₂ 121 1673.92 838.23 1674.93 837.97 558.98 113 Ac-LTF$r8AYWAQL$SAa-NH₂ 122 iso2 1673.92 838.32 1674.93 837.97 558.98 114 Ac-LTF$r8AYWAQhL$SAA-NH₂ 123 1687.93 844.37 1688.94 844.97 563.65 115 Ac-LTF$r8AYWAQhL$SAA-NH₂ 124 iso2 1687.93 844.81 1688.94 844.97 563.65 116 Ac-LTF$r8AYWEQLStSA$-NH₂ 125 1826 905.27 1827.01 914.01 609.67 117 Ac-LTF$r8AYWAQL$SLA-NH₂ 126 1715.97 858.48 1716.98 858.99 573 118 Ac-LTF$r8AYWAQL$SLA-NH₂ 127 iso2 1715.97 858.87 1716.98 858.99 573 119 Ac-LTF$r8AYWAQL$SWA-NH₂ 128 1788.96 895.21 1789.97 895.49 597.33 120 Ac-LTF$r8AYWAQL$SWA-NH₂ 129 iso2 1788.96 895.28 1789.97 895.49 597.33 121 Ac-LTF$r8AYWAQL$SVS-NH₂ 130 1717.94 859.84 1718.95 859.98 573.65 122 Ac-LTF$r8AYWAQL$SAS-NH₂ 131 1689.91 845.85 1690.92 845.96 564.31 123 Ac-LTF$r8AYWAQL$SVG-NH₂ 132 1687.93 844.81 1688.94 844.97 563.65 124 Ac-ETF$r8VYWAQL$SAa-NH₂ 133 1717.91 859.76 1718.92 859.96 573.64 125 Ac-ETF$r8VYWAQL$SAA-NH₂ 134 1717.91 859.84 1718.92 859.96 573.64 126 Ac-ETF$r8VYWAQL$SVA-NH₂ 135 1745.94 873.82 1746.95 873.98 582.99 127 Ac-ETF$r8VYWAQL$SLA-NH₂ 136 1759.96 880.85 1760.97 880.99 587.66 128 Ac-ETF$r8VYWAQL$SWA-NH₂ 137 1832.95 917.34 1833.96 917.48 611.99 129 Ac-ETF$r8KYWAQL$SWA-NH₂ 138 1861.98 931.92 1862.99 932 621.67 130 Ac-ETF$r8VYWAQL$SVS-NH₂ 139 1761.93 881.89 1762.94 881.97 588.32 131 Ac-ETF$r8VYWAQL$SAS-NH₂ 140 1733.9 867.83 1734.91 867.96 578.97 132 Ac-ETF$r8VYWAQL$SVG-NH₂ 141 1731.92 866.87 1732.93 866.97 578.31 133 Ac-LTF$r8VYWAQL$SSa-NH₂ 142 1717.94 859.47 1718.95 859.98 573.65 134 Ac-ETF$r8VYWAQL$SSa-NH₂ 143 1733.9 867.83 1734.91 867.96 578.97 135 Ac-LTF$r8VYWAQL$SNa-NH₂ 144 1744.96 873.38 1745.97 873.49 582.66 136 Ac-ETF$r8VYWAQL$SNa-NH₂ 145 1760.91 881.3 1761.92 881.46 587.98 137 Ac-LTF$r8VYWAQL$SAa-NH₂ 146 1701.95 851.84 1702.96 851.98 568.32 138 Ac-LTF$r8VYWAQL$SVA-NH₂ 147 1729.98 865.53 1730.99 866 577.67 139 Ac-LTF$r8VYWAQL$SVA-NH₂ 148 iso2 1729.98 865.9 1730.99 866 577.67 140 Ac-LTF$r8VYWAQL$SWA-NH₂ 149 1816.99 909.42 1818 909.5 606.67 141 Ac-LTF$r8VYWAQL$SVS-NH₂ 150 1745.98 873.9 1746.99 874 583 142 Ac-LTF$r8VYWAQL$SVS-NH₂ 151 iso2 1745.98 873.9 1746.99 874 583 143 Ac-LTF$r8VYWAQL$SAS-NH₂ 152 1717.94 859.84 1718.95 859.98 573.65 144 Ac-LTF$r8VYWAQL$SAS-NH₂ 153 iso2 1717.94 859.91 1718.95 859.98 573.65 145 Ac-LTF$r8VYWAQL$SVG-NH₂ 154 1715.97 858.87 1716.98 858.99 573 146 Ac-LTF$r8VYWAQL$SVG-NH₂ 155 iso2 1715.97 858.87 1716.98 858.99 573 147 Ac-LTF$r8EYWAQCha$SAA-NH₂ 156 1771.96 886.85 1772.97 886.99 591.66 148 Ac-LTF$r8EYWAQCha$SAA-NH₂ 157 iso2 1771.96 886.85 1772.97 886.99 591.66 149 Ac-LTF$r8EYWAQCpg$SAA-NH₂ 158 1743.92 872.86 1744.93 872.97 582.31 150 Ac-LTF$r8EYWAQCpg$SAA-NH₂ 159 iso2 1743.92 872.86 1744.93 872.97 582.31 151 Ac-LTF$r8EYWAQF$SAA-NH₂ 160 1765.91 883.44 1766.92 883.96 589.64 152 Ac-LTF$r8EYWAQF$SAA-NH₂ 161 iso2 1765.91 883.89 1766.92 883.96 589.64 153 Ac-LTF$r8EYWAQCba$SAA-NH₂ 162 1743.92 872.42 1744.93 872.97 582.31 154 Ac-LTF$r8EYWAQCba$SAA-NH₂ 163 iso2 1743.92 873.39 1744.93 872.97 582.31 155 Ac-LTF3C1$r8EYWAQL$SAA-NH₂ 164 1765.89 883.89 1766.9 883.95 589.64 156 Ac-LTF3C1$r8EYWAQL$SAA-NH₂ 165 iso2 1765.89 883.96 1766.9 883.95 589.64 157 Ac-LTF34F2$r8EYWAQL$SAA-NH₂ 166 1767.91 884.48 1768.92 884.96 590.31 158 Ac-LTF34F2$r8EYWAQL$SAA-NH₂ 167 iso2 1767.91 884.48 1768.92 884.96 590.31 159 Ac-LTF34F2$r8EYWAQhL$SAA-NH₂ 168 1781.92 891.44 1782.93 891.97 594.98 160 Ac-LTF34F2$r8EYWAQhL$SAA-NH₂ 169 iso2 1781.92 891.88 1782.93 891.97 594.98 161 Ac-ETF$r8EYWAQL$SAA-NH₂ 170 1747.88 874.34 1748.89 874.95 583.63 162 Ac-LTF$r8AYWVQL$SAA-NH₂ 171 1701.95 851.4 1702.96 851.98 568.32 163 Ac-LTF$r8AHWAQL$SAA-NH₂ 172 1647.91 824.83 1648.92 824.96 550.31 164 Ac-LTF$r8AEWAQL$SAA-NH₂ 173 1639.9 820.39 1640.91 820.96 547.64 165 Ac-LTF$r8ASWAQL$SAA-NH₂ 174 1597.89 799.38 1598.9 799.95 533.64 166 Ac-LTF$r8AEWAQL$SAA-NH₂ 175 iso2 1639.9 820.39 1640.91 820.96 547.64 167 Ac-LTF$r8ASWAQL$SAA-NH₂ 176 iso2 1597.89 800.31 1598.9 799.95 533.64 168 Ac-LTF$r8AF4coohWAQL$SAA-NH₂ 177 1701.91 851.4 1702.92 851.96 568.31 169 Ac-LTF$r8AF4coohWAQL$SAA-NH₂ 178 iso2 1701.91 851.4 1702.92 851.96 568.31 170 Ac-LTF$r8AHWAQL$AAIa-NH₂ 179 1745 874.13 1746.01 873.51 582.67 171 Ac-ITF$r8FYWAQL$AAIa-NH₂ 180 1847.04 923.92 1848.05 924.53 616.69 172 Ac-ITF$r8EHWAQL$AAIa-NH₂ 181 1803.01 903.17 1804.02 902.51 602.01 173 Ac-ITF$r8EHWAQL$AAIa-NH₂ 182 iso2 1803.01 903.17 1804.02 902.51 602.01 174 Ac-ETF$r8EHWAQL$AAIa-NH₂ 183 1818.97 910.76 1819.98 910.49 607.33 175 Ac-ETF$r8EHWAQL$AAIa-NH₂ 184 iso2 1818.97 910.85 1819.98 910.49 607.33 176 Ac-LTF$r8AHWVQL$AAIa-NH₂ 185 1773.03 888.09 1774.04 887.52 592.02 177 Ac-ITF$r8FYWVQL$AAIa-NH₂ 186 1875.07 939.16 1876.08 938.54 626.03 178 Ac-ITF$r8EYWVQL$AAIa-NH₂ 187 1857.04 929.83 1858.05 929.53 620.02 179 Ac-ITF$r8EHWVQL$AAIa-NH₂ 188 1831.04 916.86 1832.05 916.53 611.35 180 Ac-LTF$r8AEWAQL$AAIa-NH₂ 189 1736.99 869.87 1738 869.5 580 181 Ac-LTF$r8AF4coohWAQL$AAIa-NH₂ 190 1799 900.17 1800.01 900.51 600.67 182 Ac-LTF$r8AF4coohWAQL$AAIa-NH₂ 191 iso2 1799 900.24 1800.01 900.51 600.67 183 Ac-LTF$r8AHWAQL$AHFA-NH₂ 192 1845.01 923.89 1846.02 923.51 616.01 184 Ac-ITF$r8FYWAQL$AHFA-NH₂ 193 1947.05 975.05 1948.06 974.53 650.02 185 Ac-ITF$r8FYWAQL$AHFA-NH₂ 194 iso2 1947.05 976.07 1948.06 974.53 650.02 186 Ac-ITF$r8FHWAQL$AEFA-NH₂ 195 1913.02 958.12 1914.03 957.52 638.68 187 Ac-ITF$r8FHWAQL$AEFA-NH₂ 196 iso2 1913.02 957.86 1914.03 957.52 638.68 188 Ac-ITF$r8EHWAQLSAHFA-NH₂ 197 1903.01 952.94 1904.02 952.51 635.34 189 Ac-ITF$r8EHWAQL$AHFA-NH₂ 198 iso2 1903.01 953.87 1904.02 952 51 635.34 190 Ac-LTFSr8AHWVQL$AHFA-NH₂ 199 1873.04 937.86 1874.05 937.53 625.35 191 Ac-ITF$r8FYWVQL$AHFA-NH₂ 200 1975.08 988.83 1976.09 988.55 659.37 192 Ac-ITF$r8EYWV0L$AHFA-NH₂ 201 1957.05 979.35 1958.06 979.53 653.36 193 Ac-ITF$r8EHWVQL$AHFA-NH₂ 202 1931.05 967 1932.06 966.53 644.69 194 Ac-ITF$r8EHWVQL$AHFA-NH₂ 203 iso2 1931.05 967.93 1932.06 966.53 644.69 195 Ac-ETF$r8EYWAAL$SAA-NH₂ 204 1690.86 845.85 1691.87 846.44 564.63 196 Ac-LTF$r8AYWVAL$SAA-NH₂ 205 1644.93 824.08 1645.94 823.47 549.32 197 Ac-LTF$r8AHWAAL$SAA-NH₂ 206 1590.89 796.88 1591.9 796.45 531.3 198 Ac-LTF$r8AEWAAL$SAA-NH₂ 207 1582.88 791.9 1583.89 792.45 528.63 199 Ac-LTF$r8AEWAAL$SAA-NH₂ 208 iso2 1582.88 791.9 1583.89 792.45 528.63 200 Ac-LTF$r8ASWAAL$SAA-NH₂ 209 1540.87 770.74 1541.88 771.44 514.63 201 Ac-LTF$r8ASWAAL$SAA-NH₂ 210 iso2 1540.87 770.88 1541.88 771.44 514.63 202 Ac-LTF$r8AYWAAL$AAIa-NH₂ 211 1713.99 857.39 1715 858 572.34 203 Ac-LTF$r8AYWAAL$AAla-NH₂ 212 iso2 1713.99 857.84 1715 858 572.34 204 Ac-LTF$r8AYWAAL$AHFA-NH₂ 213 1813.99 907.86 1815 908 605.67 205 Ac-LTF$r8EHWAQL$AHIa-NH₂ 214 1869.03 936.1 1870.04 935.52 624.02 206 Ac-LTF$r8EHWAQL$AHIa-NH₂ 215 iso2 1869.03 937.03 1870.04 935.52 624.02 207 Ac-LTF$r8AHWAQL$AHIa-NH₂ 216 1811.03 906.87 1812.04 906.52 604.68 208 Ac-LTF$r8EYWAQL$AHIa-NH₂ 217 1895.04 949.15 1896.05 948.53 632.69 209 Ac-LTF$r8AYWAQL$AAFa-NH₂ 218 1804.99 903.2 1806 903.5 602.67 210 Ac-LTF$r8AYWAQL$AAFa-NH₂ 219 iso2 1804.99 903.28 1806 903.5 602.67 211 Ac-LTF$r8AYWAQL$AAWa-NH₂ 220 1844 922.81 1845.01 923.01 615.67 212 Ac-LTF$r8AYWAQL$AAVa-NH₂ 221 1756.99 878.86 1758 879.5 586.67 213 Ac-LTF$r8AYWAQL$AAVa-NH₂ 222 iso2 1756.99 879.3 1758 879.5 586.67 214 Ac-LTF$r8AYWAQL$AALa-NH₂ 223 1771.01 886.26 1772.02 886.51 591.34 215 Ac-LTF$r8AYWAQL$AALa-NH₂ 224 iso2 1771.01 886.33 1772.02 886.51 591.34 216 Ac-LTF$r8EYWAQL$AAIa-NH₂ 225 1829.01 914.89 1830.02 915.51 610.68 217 Ac-LTF$r8EYWAQL$AAIa-NH₂ 226 iso2 1829.01 915.34 1830.02 915.51 610.68 218 Ac-LTF$r8EYWAQL$AAFa-NH₂ 227 1863 932.87 1864.01 932.51 622.01 219 Ac-LTF$r8EYWAQL$AAFa-NH₂ 228 iso2 1863 932.87 1864.01 932.51 622.01 220 Ac-LTF$r8EYWAQL$AAVa-NH₂ 229 1815 908.23 1816.01 908.51 606.01 221 Ac-LTF$r8EYWAQL$AAVa-NH₂ 230 iso2 1815 908.31 1816.01 908.51 606.01 222 Ac-LTFSr8EHWAQL$AAIa-NH₂ 231 1803.01 903.17 1804.02 902.51 602.01 223 Ac-LTF$r8EHWAQL$AAIa-NH₂ 232 iso2 1803.01 902.8 1804.02 902.51 602.01 224 Ac-LTF$r8EHWAQL$AAWa-NH₂ 233 1876 939.34 1877.01 939.01 626.34 225 Ac-LTF$r8EHWAQL$AAWa-NH₂ 234 iso2 1876 939.62 1877.01 939.01 626.34 226 Ac-LTF$r8EHWAQL$AALa-NH₂ 235 1803.01 902.8 1804.02 902.51 602.01 227 Ac-LTF$r8EHWAQL$AALa-NH₂ 236 iso2 1803.01 902.9 1804.02 902.51 602.01 228 Ac-ETF$r8EHWVQL$AALa-NH₂ 237 1847 924.82 1848.01 924.51 616.67 229 Ac-LTF$r8AYWAQL$AAAa-NH₂ 238 1728.96 865.89 1729.97 865.49 577.33 230 Ac-LTF$r8AYWAQL$AAAa-NH₂ 239 iso2 1728.96 865.89 1729.97 865.49 577.33 231 Ac-LTF$r8AYWAQL$AAAibA-NH₂ 240 1742.98 872.83 1743.99 872.5 582 232 Ac-LTF$r8AYWAQL$AAAibA-NH₂ 241 iso2 1742.98 872.92 1743.99 872.5 582 233 Ac-LTF$r8AYWAQL$AAAAa-NH₂ 242 1800 901.42 1801.01 901.01 601.01 234 Ac-LTF$r5AYWAQL$s8AAIa-NH₂ 243 1771.01 887.17 1772.02 886.51 591.34 235 Ac-LTF$r5AYWAQL$s8SAA-NH₂ 244 1673.92 838.33 1674.93 837.97 558.98 236 Ac-LTF$r8AYWAQCba$AANleA-NH₂ 245 1783.01 892.64 1784.02 892.51 595.34 237 Ac-ETF$r8AYWAQCba$AANleA-NH₂ 246 1798.97 900.59 1799.98 900.49 600.66 238 Ac-LTF$r8EYWAQCba$AANleA-NH₂ 247 1841.01 922.05 1842.02 921.51 614.68 239 Ac-LTF$r8AYWAQCba$AWNleA-NH₂ 248 1898.05 950.46 1899.06 950.03 633.69 240 Ac-ETF$r8AYWAQCba$AWNleA-NH₂ 249 1914.01 958.11 1915.02 958.01 639.01 241 Ac-LTF$r8EYWAQCba$AWNleA-NH₂ 250 1956.06 950.62 1957.07 979.04 653.03 242 Ac-LTF$r8EYWAQCba$SAFA-NH₂ 251 1890.99 946.55 1892 946.5 631.34 243 Ac-LTF34F2$r8EYWAQCba$SANleA-NH₂ 252 1892.99 947.57 1894 947.5 632 244 Ac-LTF$r8EF4coohWAQCba$SANleA-NH₂ 253 1885 943.59 1886.01 943.51 629.34 245 Ac-LTF$r8EYWSQCba$SANleA-NH₂ 254 1873 937.58 1874.01 937.51 625.34 246 Ac-LTF$r8EYWWQCba$SANleA-NH₂ 255 1972.05 987.61 1973.06 987.03 658.36 247 Ac-LTF$r8EYWAQCba$AAIa-NH₂ 256 1841.01 922.05 1842.02 921.51 614.68 248 Ac-LTF34F2$r8EYWAQCba$AAIa-NH₂ 257 1876.99 939.99 1878 939.5 626.67 249 Ac-LTF$r8EF4coohWAQCba$AAIa-NH₂ 258 1869.01 935.64 1870.02 935.51 624.01 250 Pam-ETF$r8EYWAQCba$SAA-NH₂ 259 1956.1 979.57 1957.11 979.06 653.04 251 Ac-LThF$r8EFWAQCba$SAA-NH₂ 260 1741.94 872.11 1742.95 871.98 581.65 252 Ac-LTA$r8EYWAQCba$SAA-NH₂ 261 1667.89 835.4 1668.9 834.95 556.97 253 Ac-LTF$r8EYAAQCba$SAA-NH₂ 262 1628.88 815.61 1629.89 815.45 543.97 254 Ac-LTF$r8EY2NalAQCba$SAA-NH₂ 263 1754.93 879.04 1755.94 878.47 585.98 255 Ac-LTF$r8AYWAQCba$SAA-NH₂ 264 1685.92 844.71 1686.93 843.97 562.98 256 Ac-LTF$r8EYWAQCba$SAF-NH₂ 265 1819.96 911.41 1820.97 910.99 607.66 257 Ac-LTF$r8EYWAQCba$SAFa-NH₂ 266 1890.99 947.41 1892 946.5 631.34 258 Ac-LTF$r8AYWAQCba$SAF-NH₂ 267 1761.95 882.73 1762.96 881.98 588.32 259 Ac-LTF34F2$r8AYWAQCba$SAF-NH₂ 268 1797.93 900.87 1798.94 899.97 600.32 260 Ac-LTF$r8AF4coohWAQCba$SAF-NH₂ 269 1789.94 896.43 1790.95 895.98 597.65 261 Ac-LTF$r8EY6clWAQCba$SAF-NH₂ 270 1853.92 929.27 1854.93 927.97 618.98 262 Ac-LTF$r8AYWSQCba$SAF-NH₂ 271 1777.94 890.87 1778.95 889.98 593.65 263 Ac-LTF$r8AYWWQCba$SAF-NH₂ 272 1876.99 939.91 1878 939.5 626.67 264 Ac-LTF$r8AYWAQCba$AAIa-NH₂ 273 1783.01 893.19 1784.02 892.51 595.34 265 Ac-LTF34F2$r8AYWAQCba$AAIa-NH₂ 274 1818.99 911.23 1820 910.5 607.34 266 Ac-LTF$r8AY6clWAQCba$AAIa-NH₂ 275 1816.97 909.84 1817.98 909.49 606.66 267 Ac-LTF$r8AF4coohWAQCba$AAIa-NH₂ 276 1811 906.88 1812.01 906.51 604.67 268 Ac-LTF$r8EYWAQCba$AAFa-NH₂ 277 1875 938.6 1876.01 938.51 626.01 269 Ac-LTF$r8EYWAQCba$AAFa-NH₂ 278 iso2 1875 938.6 1876.01 938.51 626.01 270 Ac-ETF$r8AYWAQCba$AWNlea-NH₂ 279 1914.01 958.42 1915.02 958.01 639.01 271 Ac-LTF$r8EYWAQCba$AWNlea-NH₂ 280 1956.06 979.42 1957.07 979.04 653.03 272 Ac-ETF$r8EYWAQCba$AWNlea-NH₂ 281 1972.01 987.06 1973.02 987.01 658.34 273 Ac-ETF$r8EYWAQCba$AWNlea-NH₂ 282 iso2 1972.01 987.06 1973.02 987.01 658.34 274 Ac-LTF$r8AYWAQCba$SAFa-NH₂ 283 1832.99 917.89 1834 917.5 612 275 Ac-LTF$r8AYWAQCba$SAFa-NH₂ 284 iso2 1832.99 918.07 1834 917.5 612 276 Ac-ETF$r8AYWAQL$AWNlea-NH₂ 285 1902.01 952.22 1903.02 952.01 635.01 277 Ac-LTF$r8EYWAQL$AWNlea-NH₂ 286 1944.06 973.5 1945.07 973.04 649.03 278 Ac-ETF$r8EYWAQL$AWNlea-NH₂ 287 1960.01 981.46 1961.02 981.01 654.34 279 Dmaac-LTF$r8EYWAQhL$SAA-NH₂ 288 1788.98 896.06 1789.99 895.5 597.33 280 Hexac-LTF$r8EYWAQhL$SAA-NH₂ 289 1802 902.9 1803.01 902.01 601.67 281 Napac-LTF$r8EYWAQhL$SAA-NH₂ 290 1871.99 937.58 1873 937 625 282 Decac-LTF$r8EYWAQhL$SAA-NH₂ 291 1858.06 930.55 1859.07 930.04 620.36 283 Admac-LTF$r8EYWAQhL$SAA-NH₂ 292 1866.03 934.07 1867.04 934.02 623.02 284 Tmac-LTF$r8EYWAQhL$SAA-NH₂ 293 1787.99 895.41 1789 895 597 285 Pam-LTF$r8EYWAQhL$SAA-NH₂ 294 1942.16 972.08 1943.17 972.09 648.39 286 Ac-LTF$r8AYWAQCba$AANleA-NH₂ 295 iso2 1783.01 892.64 1784.02 892.51 595.34 287 Ac-LTF34F2$r8EYWAQCba$AAIa-NH₂ 296 iso2 1876.99 939.62 1878 939.5 626.67 288 Ac-LTF34F2$r8EYWAQCba$SAA-NH₂ 297 1779.91 892.07 1780.92 890.96 594.31 289 Ac-LTF34F2$r8EYWAQCba$SAA-NH₂ 298 iso2 1779.91 891.61 1780.92 890.96 594.31 290 Ac-LTF$r8EF4coohWAQCba$SAA-NH₂ 299 1771.92 887.54 1772.93 886.97 591.65 291 Ac-LTF$r8EF4coohWAQCba$SAA-NH₂ 300 iso2 1771.92 887.63 1772.93 886.97 591.65 292 Ac-LTF$r8EYWSQCba$SAA-NH₂ 301 1759.92 881.9 1760.93 880.97 587.65 293 Ac-LTF$r8EYWSQCba$SAA-NH₂ 302 iso2 1759.92 881.9 1760.93 880.97 587.65 294 Ac-LTF$r8EYWAQhL$SAA-NH₂ 303 1745.94 875.05 1746.95 873.98 582.99 295 Ac-LTFSrHAYWAQhL$SAF-NH₂ 304 1763.97 884.02 1764.98 882.99 589 296 Ac-LTF$r8AYWAQhL$SAF-NH₂ 305 iso2 1763.97 883.56 1764.98 882.99 589 297 Ac-LTF34F2$r8AYWAQhL$SAA-NH₂ 306 1723.92 863.67 1724.93 862 97 575.65 298 Ac-LTF34F2$r8AYWAQhL$SAA-NH₂ 307 iso2 1723.92 864.04 1724.93 862.97 575.65 299 Ac-LTF$r8AF4coohWAQhL$SAA-NH₂ 308 1715.93 859.44 1716.94 858.97 572.98 300 Ac-LTF$r8AF4coohWAQhL$SAA-NH₂ 309 iso2 1715.93 859.6 1716.94 858.97 572.98 301 Ac-LTF$r8AYWSQhL$SAA-NH₂ 310 1703.93 853.96 1704.94 852.97 568.98 302 Ac-LTF$r8AYWSQhL$SAA-NH₂ 311 iso2 1703.93 853.59 1704.94 852.97 568.98 303 Ac-LTF$r8EYWAQL$AANleA-NH₂ 312 1829.01 915.45 1830.02 915.51 610.68 304 Ac-LTF34F2$r8AYWAQL$AANleA-NH₂ 313 1806.99 904.58 1808 904.5 603.34 305 Ac-LTF$r8AF4coohWAQL$AANleA-NH₂ 314 1799 901.6 1800.01 900.51 600.67 306 Ac-LTF$r8AYWSQL$AANleA-NH₂ 315 1787 894.75 1788.01 894.51 596.67 307 Ac-LTF34F2$r8AYWAQhL$AANleA-NH₂ 316 1821 911.79 1822.01 911.51 608.01 308 Ac-LTF34F2$r8AYWAQhL$AANleA-NH₂ 317 iso2 1821 912.61 1822.01 911.51 608.01 309 Ac-LTF$r8AF4coohWAQhL$AANleA-NH₂ 318 1813.02 907.95 1814.03 907.52 605.35 310 Ac-LTF$r8AF4coohWAQhL$AANleA-NH₂ 319 iso2 1813.02 908.54 1814.03 907.52 605.35 311 Ac-LTFSr8AYWSQhL$AANleA-NH₂ 320 1801.02 901.84 1802.03 901.52 601.35 312 Ac-LTF$r8AYWSQhL$AANleA-NH₂ 321 iso2 1801.02 902.62 1802.03 901.52 601.35 313 Ac-LTF$r8AYWAQhL$AAAAa-NH₂ 322 1814.01 908.63 1815.02 908.01 605.68 314 Ac-LTF$r8AYWAQhL$AAAAa-NH₂ 323 iso2 1814.01 908.34 1815.02 908.01 605.68 315 Ac-LTF$r8AYWAQL$AAAAAa-NH₂ 324 1871.04 936.94 1872.05 936.53 624.69 316 Ac-LTF$r8AYWAQL$AAAAAAa-NH₂ 325 iso2 1942.07 972.5 1943.08 972.04 648.37 317 Ac-LTF$r8AYWAQL$AAAAAAa-NH₂ 326 iso1 1942.07 972.5 1943.08 972.04 648.37 318 Ac-LTF$r8EYWAQhL$AANleA-NH₂ 327 1843.03 922.54 1844.04 922.52 615.35 319 Ac-AATF$r8AYWAQL$AANleA-NH₂ 328 1800 901.39 1801.01 901.01 601.01 320 Ac-LTF$r8AYWAQL$AANleAA-NH₂ 329 1842.04 922.45 1843.05 922.03 615.02 321 Ac-ALTF$r8AYWAQL$AANleAA-NH₂ 330 1913.08 957.94 1914.09 957.55 638.7 322 Ac-LTF$r8AYWAQCba$AANleAA-NH₂ 331 1854.04 928.43 1855.05 928.03 619.02 323 Ac-LTF$r8AYWAQhL$AANleAA-NH₂ 332 1856.06 929.4 1857.07 929.04 619.69 324 Ac-LTF$r8EYWAQCba$SAAA-NH₂ 333 1814.96 909.37 1815.97 908.49 605.99 325 Ac-LTF$r8EYWAQCba$SAAA-NH₂ 334 iso2 1814.96 909.37 1815.97 908.49 605.99 326 Ac-LTF$r8EYWAQCba$SAAAA-NH₂ 335 1886 944.61 1887.01 944.01 629.67 327 Ac-LTF$r8EYWAQCba$SAAAA-NH₂ 336 iso2 1886 944.61 1887.01 944.01 629.67 328 Ac-ALTF$r8EYWAQCba$SAA-NH₂ 337 1814.96 909.09 1815.97 908.49 605.99 329 Ac-ALTF$r8EYWAQCba$SAAA-NH₂ 338 1886 944.61 1887.01 944.01 629.67 330 Ac-ALTF$r8EYWAQCba$SAA-NH₂ 339 iso2 1814.96 909.09 1815.97 908.49 605.99 331 Ac-LTF$r8EYWAQL$AAAAAa-NH₂ 340 iso2 1929.04 966.08 1930.05 965.53 644.02 332 Ac-LTF$r8EY6clWAQCba$SAA- 341 1777.89 890.78 1778.9 889.95 593.64 333 Ac-LTF$r8EF4cooh6clWAQCba$SANleA-NH₂ 342 1918.96 961.27 1919.97 960.49 640.66 334 Ac-LTF$r8EF4cooh6clWAQCba$SANleA-NH₂ 343 iso2 1918.96 961.27 1919.97 960.49 640.66 335 Ac-LTF$r8EF4cooh6clWAQCba$AAIa-NH₂ 344 1902.97 953.03 1903.98 952.49 635.33 336 Ac-LTF$r8EF4cooh6clWAQCba$AAla-NH₂ 345 iso2 1902.97 953.13 1903.98 952.49 635.33 337 Ac-LTF$r8AY6clWAQL$AAAAAa-NH₂ 346 1905 954.61 1906.01 953.51 636.01 338 Ac-LTF$r8AY6clWAQL$AAAAAa-NH₂ 347 iso2 1905 954.9 1906.01 953.51 636.01 339 Ac-F$r8AY6clWEAL$AAAAAAa-NH₂ 348 1762.89 883.01 1763.9 882.45 588.64 340 Ac-ETF$r8EYWAQL$AAAAAa-NH₂ 349 1945 974.31 1946.01 973.51 649.34 341 Ac-ETF$r8EYWAQL$AAAAAa-NH₂ 350 iso2 1945 974.49 1946.01 973.51 649.34 342 Ac-LTF$r8EYWAQL$AAAAAAa-NH₂ 351 2000.08 1001.6 2001.09 1001.05 667.7 343 Ac-LTF$r8EYWAQL$AAAAAAa-NH₂ 352 iso2 2000.08 1001.6 2001.09 1001.05 667.7 344 Ac-LTF$r8AYWAQL$AANleAAa-NH₂ 353 1913.08 958.58 1914.09 957.55 638.7 345 Ac-LTF$r8AYWAQL$AANleAAa-NH₂ 354 iso2 1913.08 958.58 1914.09 957.55 638.7 346 Ac-LTF$r8EYWAQCba$AAAAAa-NH₂ 355 1941.04 972.55 1942.05 971.53 648.02 347 Ac-LTF$r8EYWAQCba$AAAAAa-NH₂ 356 iso2 1941.04 972.55 1942.05 971.53 648.02 348 Ac-LTFSr8EF4coohWAQCba$AAAAAa-NH₂ 357 1969.04 986.33 1970.05 985.53 657.35 349 Ac-LTF$r8EF4coohWAQCba$AAAAAa-NH₂ 358 iso2 1969.04 986.06 1970.05 985.53 657.35 350 Ac-LTF$r8EYWSQCba$AAAAAa-NH₂ 359 1957.04 980.04 1958.05 979.53 653.35 351 Ac-LTF$r8EYWSQCba$AAAAAa-NH₂ 360 iso2 1957.04 980.04 1958.05 979.53 653.35 352 Ac-LTF$r8EYWAQCba$SAAa-NH₂ 361 1814.96 909 1815.97 908.49 605.99 353 Ac-LTF$r8EYWAQCba$SAAa-NH₂ 362 iso2 1814.96 909 1815.97 908.49 605.99 354 Ac-ALTF$r8EYWAQCba$SAAa-NH₂ 363 1886 944.52 1887.01 944.01 629.67 355 Ac-ALTF$r8EYWAQCba$SAAa-NH₂ 364 iso2 1886 944.98 1887.01 944.01 629.67 356 Ac-ALTF$r8EYWAQCba$SAAAa-NH₂ 365 1957.04 980.04 1958.05 979.53 653.35 357 Ac-ALTF$r8EYWAQCba$SAAAa-NH₂ 366 iso2 1957.04 980.04 1958.05 979.53 653.35 358 Ac-AALTF$r8EYWAQCba$SAAAa-NH₂ 367 2028.07 1016.1 2029.08 1015.04 677.03 359 Ac-AALTF$r8EYWAQCba$SAAAa-NH₂ 368 iso2 2028.07 1015.57 2029.08 1015.04 677.03 360 Ac-RTF$r8EYWAQCba$SAA-NH₂ 369 1786.94 895.03 1787.95 894.48 596.65 361 Ac-LRF$r8EYWAQCba$SAA-NH₂ 370 1798.98 901.51 1799.99 900.5 600.67 362 Ac-LTF$r8EYWRQCba$SAA-NH₂ 371 1828.99 916.4 1830 915.5 610.67 363 Ac-LTF$r8EYWARCba$SAA-NH₂ 372 1771.97 887.63 1772.98 886.99 591.66 364 Ac-LTF$r8EYWAQCba$RAA-NH₂ 373 1812.99 908.08 1814 907.5 605.34 365 Ac-LTF$r8EYWAQCba$SRA-NH₂ 374 1828.99 916.12 1830 915.5 610.67 366 Ac-LTF$r8EYWAQCba$SAR-NH₂ 375 1828.99 916.12 1830 915.5 610.67 367 5-FAM-BaLTF$r8EYWAQCba$SAA-NH₂ 376 2131 1067.09 2132.01 1066.51 711.34 368 5-FAM-BaLTF$r8AYWAQL$AANleA-NH₂ 377 2158.08 1080.6 2159.09 1080.05 720.37 369 Ac-LAF$r8EYWAQL$AANleA-NH₂ 378 1799 901.05 1800.01 900.51 600.67 370 Ac-ATF$r8EYWAQL$AANleA-NH₂ 379 1786.97 895.03 1787.98 894.49 596.66 371 Ac-AAF$r8EYWAQL$AANleA-NH₂ 380 1756.96 880.05 1757.97 879.49 586.66 372 Ac-AAAF$r8EYWAQL$AANleA-NH₂ 381 1827.99 915.57 1829 915 610.34 373 Ac-AAAAF$r8EYWAQL$AANleA-NH₂ 382 1899.03 951.09 1900.04 950.52 634.02 374 Ac-AATF$r8EYWAQL$AANleA-NH₂ 383 1858 930.92 1859.01 930.01 620.34 375 Ac-AALTF$r8EYWAQL$AANleA-NH₂ 384 1971.09 987.17 1972.1 986.55 658.04 376 Ac-AAALTF$r8EYWAQL$AANleA-NH₂ 385 2042.12 1023.15 2043.13 1022.07 681.71 377 Ac-LTF$r8EYWAQL$AANleAA-NH₂ 386 1900.05 952.02 1901.06 951.03 634.36 378 Ac-ALTF$r8EYWAQL$AANleAA-NH₂ 387 1971.09 987.63 1972.1 986.55 658.04 379 Ac-AALTF$r8EYWAQL$AANleAA-NH₂ 388 2042.12 1022.69 2043.13 1022.07 681.71 380 Ac-LTF$r8EYWAQCba$AANleAA-NH₂ 389 1912.05 958.03 1913.06 957.03 638.36 381 Ac-LTF$r8EYWAQhL$AANleAA-NH₂ 390 1914.07 958.68 1915.08 958.04 639.03 382 Ac-ALTF$r8EYWAQhL$AANleAA-NH₂ 391 1985.1 994.1 1986.11 993.56 662.71 383 Ac-LTF$r8ANmYWAQL$AANleA-NH₂ 392 1785.02 894.11 1786.03 893.52 596.01 384 Ac-LTF$r8ANmYWAQL$AANleA-NH₂ 393 iso2 1785.02 894.11 1786.03 893.52 596.01 385 Ac-LTF$r8AYNmWAQL$AANleA-NH₂ 394 1785.02 894.11 1786.03 893.52 596.01 386 Ac-LTF$r8AYNmWAQL$AANleA-NH₂ 395 iso2 1785.02 894.11 1786.03 893.52 596.01 387 Ac-LTF$r8AYAmwAQL$AANleA-NH₂ 396 1785.02 894.01 1786.03 893.52 596.01 388 Ac-LTF$r8AYAmwAQL$AANleA-NH₂ 397 iso2 1785.02 894.01 1786.03 893.52 596.01 389 Ac-LTF$r8AYWAibQL$AANleA-NH₂ 398 1785.02 894.01 1786.03 893.52 596.01 390 Ac-LTF$r8AYWAibQL$AANleA-NH₂ 399 iso2 1785.02 894.01 1786.03 893.52 596.01 391 Ac-LTF$r8AYWAQL$AAibNleA-NH₂ 400 1785.02 894.38 1786.03 893.52 596.01 392 Ac-LTF$r8AYWAQL$AAibNleA-NH₂ 401 iso2 1785.02 894.38 1786.03 893.52 596.01 393 Ac-LTF$r8AYWAQL$AaNleA-NH₂ 402 1771.01 887.54 1772.02 886.51 591.34 394 Ac-LTF$r8AYWAQL$AaNleA-NH₂ 403 iso2 1771.01 887.54 1772.02 886.51 591.34 395 Ac-LTF$r8AYWAQL$ASarNleA-NH₂ 404 1771.01 887.35 1772.02 886.51 591.34 396 Ac-LTF$r8AYWAQL$ASarNleA-NH₂ 405 iso2 1771.01 887.35 1772.02 886.51 591.34 397 Ac-LTF$r8AYWAQL$AANleAib-NH₂ 406 1785.02 894.75 1786.03 893.52 596.01 398 Ac-LTF$r8AYWAQL$AANleAib-NH₂ 407 iso2 1785.02 894.75 1786.03 893.52 596.01 399 Ac-LTF$r8AYWAQL$AANleNmA-NH₂ 408 1785.02 894.6 1786.03 893.52 596.01 400 Ac-LTF$r8AYWAQL$AANleNmA-NH₂ 409 iso2 1785.02 894.6 1786.03 893.52 596.01 401 Ac-LTF$r8AYWAQL$AANleSar-NH₂ 410 1771.01 886.98 1772.02 886.51 591.34 402 Ac-LTF$r8AYWAQL$AANleSar-NH₂ 411 iso2 1771.01 886.98 1772.02 886.51 591.34 403 Ac-LTF$r8AYWAQL$AANleAAib-NH₂ 412 1856.06 1857.07 929.04 619.69 404 Ac-LTF$r8AYWAQL$AANleAAib-NH₂ 413 iso2 1856.06 1857.07 929.04 619.69 405 Ac-LTF$r8AYWAQL$AANleANmA-NH₂ 414 1856.06 930.37 1857.07 929.04 619.69 406 Ac-LTF$r8AYAATAQL$AANleANmA-NH₂ 415 iso2 1856.06 930.37 1857.07 929.04 619.69 407 Ac-LTF$r8AYWAQL$AANleAa-NH₂ 416 1842.04 922.69 1843.05 922.03 615.02 408 Ac-LTF$r8AYWAQL$AANleAa-NH₂ 417 iso2 1842.04 922.69 1843.05 922.03 615.02 409 Ac-LTF$r8AYWAQL$AANleASar-NH₂ 418 1842.04 922.6 1843.05 922.03 615.02 410 Ac-LTF$r8AYWAQL$AANleASar-NH₂ 419 iso2 1842.04 922.6 1843.05 922.03 615.02 411 Ac-LTF$/r8AYWAQL$/AANleA-NH₂ 420 1799.04 901.14 1800.05 900.53 600.69 412 Ac-LTFAibAYWAQLAibAANleA-NH₂ 421 1648.9 826.02 1649.91 825.46 550.64 413 Ac-LTF$r8Cou4YWAQL$AANleA-NH₂ 422 1975.05 989.11 1976.06 988.53 659.36 414 Ac-LTF$r8Cou4YWAQL$AANleA-NH₂ 423 iso2 1975.05 989.11 1976.06 988.53 659.36 415 Ac-LTF$r8AYWCou4QL$AANleA-NH₂ 424 1975.05 989.11 1976.06 988.53 659.36 416 Ac-LTF$r8AYWAQL$Cou4ANleA-NH₂ 425 1975.05 989.57 1976.06 988.53 659.36 417 Ac-LTF$r8AYWAQL$Cou4ANleA-NH₂ 426 iso2 1975.05 989.57 1976.06 988.53 659.36 418 Ac-LTF$r8AYWAQL$ACou4NleA-NH₂ 427 1975.05 989.57 1976.06 988.53 659.36 419 Ac-LTF$r8AYWAQL$ACou4NleA-NH₂ 428 iso2 1975.05 989.57 1976.06 988.53 659.36 420 Ac-LTF$r8AYWAQL$AANleA-OH 429 1771.99 887.63 1773 887 591.67 421 Ac-LTF$r8AYWAQL$AANleA-OH 430 iso2 1771.99 887.63 1773 887 591.67 422 Ac-LTF$r8AYWAQL$AANleA-NHnPr 431 1813.05 908.08 1814.06 907.53 605.36 423 Ac-LTF$r8AYWAQL$AANleA-NHnPr 432 iso2 1813.05 908.08 1814.06 907.53 605.36 424 Ac-LTF$r8AYWAQL$AANleA-NHnBu33Me 433 1855.1 929.17 1856.11 928.56 619.37 425 Ac-LTF$r8AYWAQL$AANleA-NHnBu33Me 434 iso2 1855.1 929.17 1856.11 928.56 619.37 426 Ac-LTF$r8AYWAQL$AANleA-NHHex 435 1855.1 929.17 1856.11 928.56 619.37 427 Ac-LTF$r8AYWAQL$AANleA-NHHex 436 iso2 1855.1 929.17 1856.11 928.56 619.37 428 Ac-LTA$r8AYWAQL$AANleA-NH₂ 437 1694.98 849.33 1695.99 848.5 566 429 Ac-LThL$r8AYWAQL$AANleA-NH₂ 438 1751.04 877.09 1752.05 876.53 584.69 430 Ac-LTF$r8AYAAQL$AANleA-NH₂ 439 1655.97 829.54 1656.98 828.99 553 431 Ac-LTF$r8AY2Na1AQL$AANleA-NH₂ 440 1782.01 892.63 1783.02 892.01 595.01 432 Ac-LTF$r8EYWCou4QCba$SAA-NH₂ 441 1947.97 975.8 1948.98 974.99 650.33 433 Ac-LTF$r8EYWCou7QCba$SAA-NH₂ 442 16.03 974.9 17.04 9.02 6.35 434 Ac-LTF%r8EYWAQCba%SAA-NH₂ 443 1745.94 874.8 1746.95 873.98 582.99 435 Dmaac-LTF$r8EYWAQCba$SAA-NH₂ 444 1786.97 894.8 1787.98 894.49 596.66 436 Dmaac-LTF$r8AYWAQL$AAAAAa-NH₂ 445 1914.08 958.2 1915.09 958.05 639.03 437 Dmaac-LTF$r8AYWAQL$AAAAAa-NH₂ 446 iso2 1914.08 958.2 1915.09 958.05 639.03 438 Dmaac-LTF$r8EYWAQL$AAAAAa-NH₂ 447 1972.08 987.3 1973.09 987.05 658.37 439 Dmaac-LTF$r8EYWAQL$AAAAAa-NH₂ 448 iso2 1972.08 987.3 1973.09 987.05 658.37 440 Dmaac-LTF$r8EF4coohWAQCba$AAIa-NH₂ 449 1912.05 957.4 1913.06 957.03 638.36 441 Dmaac-LTF$r8EF4coohWAQCba$AAIa-NH₂ 450 iso2 1912.05 957.4 1913.06 957.03 638.36 442 Dmaac-LTF$r8AYWAQL$AANleA-NH₂ 451 1814.05 908.3 1815.06 908.03 605.69 443 Dmaac-LTF$r8AYWAQL$AANleA-NH₂ 452 iso2 1814.05 908.3 1815.06 908.03 605.69 444 Ac-LTF%r8AYWAQL%AANleA-NH₂ 453 1773.02 888.37 1774.03 887.52 592.01 445 Ac-LTF%r8EYWAQL%AAAAAa-NH₂ 454 1931.06 966.4 1932.07 966.54 644.69 446 Cou6BaLTF$r8EYWAQhL$SAA-NH₂ 455 2018.05 1009.9 2019.06 1010.03 673.69 447 Cou8BaLTF$r8EYWAQhL$SAA-NH₂ 456 1962.96 982.34 1963.97 982.49 655.32 448 Ac-LTF4M8EYWAQL$AAAAAa-NH₂ 457 2054.93 1028.68 2055.94 1028.47 685.98 449 Ac-LTF$r8EYWAQL$AAAAAa-NH₂ 458 1929.04 966.17 1930.05 965.53 644.02 550 Ac-LTF$r8EYWAQL$AAAAAa-OH 459 1930.02 966.54 1931.03 966.02 644.35 551 Ac-LTF$r8EYWAQL$AAAAAa-OH 460 iso2 1930.02 965.89 1931.03 966.02 644.35 552 Ac-LTF$r8EYWAEL$AAAAAa-NH₂ 461 1930.02 966.82 1931.03 966.02 644.35 553 Ac-LTF$r8EYWAEL$AAAAAa-NH₂ 462 iso2 1930.02 966.91 1931.03 966.02 644.35 554 Ac-LTF$r8EYWAEL$AAAAAa-OH 463 1931.01 967.28 1932.02 966.51 644.68 555 Ac-LTF$r8EY6clWAQL$AAAAAa-NH₂ 464 1963 983.28 1964.01 982.51 655.34 556 Ac-LTF$r8EF4bOH2WAQL$AAAAAa-NH₂ 465 1957.05 980.04 1958.06 979.53 653.36 557 Ac-AAALTF$r8EYWAQL$AAAAAa-NH₂ 466 2142.15 1072.83 2143.16 1072.08 715.06 558 Ac-LTF34F2$r8EYWAQL$AAAAAa-NH₂ 467 1965.02 984.3 1966.03 983.52 656.01 559 Ac-RTF$r8EYWAQL$AAAAAa-NH₂ 468 1972.06 987.81 1973.07 987.04 658.36 560 Ac-LTA$r8EYWAQL$AAAAAa-NH₂ 469 1853.01 928.33 1854.02 927.51 618.68 561 Ac-LTF$r8EYWAibQL$AAAAAa-NH₂ 470 1943.06 973.48 1944.07 972.54 648.69 562 Ac-LTF$r8EYWAQLSAAibAAAa-NH₂ 471 1943.06 973.11 1944.07 972.54 648.69 563 Ac-LTF$r8EYWAQL$AAAibAAa-NH₂ 472 1943.06 973.48 1944.07 972.54 648.69 564 Ac-LTF$r8EYWAQL$AAAAibAa-NH₂ 473 1943.06 973.48 1944.07 972.54 648.69 565 Ac-LTF$r8EYWAQL$AAAAAiba-NH₂ 474 1943.06 973.38 1944.07 972.54 648.69 566 Ac-LTF$r8EYWAQL$AAAAAiba-NH₂ 475 iso2 1943.06 973.38 1944.07 972.54 648.69 567 Ac-LTF$r8EYWAQL$AAAAAAib-NH₂ 476 1943.06 973.01 1944.07 972.54 648.69 568 Ac-LTF$r8EYWAQL$AaAAAa-NH₂ 477 1929.04 966.54 1930.05 965.53 644.02 569 Ac-LTF$r8EYWAQL$AAaAAa-NH₂ 478 1929.04 966.35 1930.05 965.53 644.02 570 Ac-LTF$r8EYWAQL$AAAaAa-NH₂ 479 1929.04 966.54 1930.05 965.53 644.02 571 Ac-LTF$r8EYWAQL$AAAaAa-NH₂ 480 iso2 1929.04 966.35 1930.05 965.53 644.02 572 Ac-LTF$r8EYWAQL$AAAAaa-NH₂ 481 1929.04 966.35 1930.05 965.53 644.02 573 Ac-LTF$r8EYWAQL$AAAAAA-NH₂ 482 1929.04 966.35 1930.05 965.53 644.02 574 Ac-LTF$r8EYWAQL$ASarAAAa-NH₂ 483 1929.04 966.54 1930.05 965.53 644.02 575 Ac-LTF$r8EYWAQL$AASarAAa-NH₂ 484 1929.04 966.35 1930.05 965.53 644.02 576 Ac-LTF$r8EYWAQL$AAASarAa-NH₂ 485 1929.04 966.35 1930.05 965.53 644.02 577 Ac-LTF$r8EYWAQL$AAAASara-NH₂ 486 1929.04 966.35 1930.05 965.53 644 02 578 Ac-LTF$r8EYWAQL$AAAAASar-NH₂ 487 1929.04 966.08 1930.05 965.53 644.02 579 Ac-7LTF$r8EYWAQL$AAAAAa-NH₂ 488 1918.07 951.99 1919.08 960.04 640.37 581 Ac-TF$r8EYWAQL$AAAAAa-NH₂ 489 1815.96 929.85 1816.97 908.99 606.33 582 Ac-F$r8EYWAQL$AAAAAa-NH₂ 490 1714.91 930.92 1715.92 858.46 572.64 583 Ac-LVF$r8EYWAQL$AAAAAa-NH₂ 491 1927.06 895.12 1928.07 964.54 643.36 584 Ac-AAF$r8FYWAQL$AAAAAa-NH₂ 492 1856.98 859.51 1857.99 929.5 620 585 Ac-LTF$r8FYWAQL$AAAAa-NH₂ 493 1858 824.08 1859.01 930.01 620.34 586 Ac-LTF$rSEYWAQL$AAAa-NH₂ 494 1786.97 788.56 1787.98 894.49 596.66 587 Ac-LTF$r8EYWAQL$AAa-NH₂ 495 1715.93 1138.57 1716.94 858.97 572.98 588 Ac-LTF$r8EYWAQL$Aa-NH₂ 496 1644.89 1144.98 1645.9 823.45 549.3 589 Ac-LTF$r8EYWAQL$a-NH₂ 497 1573.85 1113.71 1574.86 787.93 525.62 590 Ac-LTF$r8EYWAQL$AAA-OH 498 1716.91 859.55 1717.92 859.46 573.31 591 Ac-LTF$r8EYWAQL$A-OH 499 1574.84 975.14 1575.85 788.43 525.95 592 Ac-LTF$r8EYWAQL$AAA-NH₂ 500 1715.93 904.75 1716.94 858.97 572.98 593 Ac-LTF$r8EYWAQCba$SAA-OH 501 1744.91 802.49 1745.92 873.46 582.64 594 Ac-LTF$r8EYWAQCba$S-OH 502 1602.83 913.53 1603.84 802.42 535.28 595 Ac-LTF$r8EYWAQCba$S-NH₂ 503 1601.85 979.58 1602.86 801.93 534.96 596 4-FBzl-LTF$r8EYWAQL$AAAAAa-NH₂ 504 2009.05 970.52 2010.06 1005.53 670.69 597 4-FBzl-LTF$r8EYWAQCba$SAA-NH₂ 505 1823.93 965.8 1824.94 912.97 608.98 598 Ac-LTF$r8RYWAQL$AAAAAa-NH₂ 506 1956.1 988.28 1957.11 979.06 653.04 599 Ac-LTF$r8HYWAQL$AAAAAa-NH₂ 507 1437.06 1003.54 1938.07 969.54 646.69 600 Ac-LTF$r8QYWAQL$AAAAAa-NH₂ 508 1928.06 993.92 1929.07 965.04 643.69 601 Ac-LTF$r8CitYWAQL$AAAAAa-NH₂ 509 1957.08 987 1958.09 979.55 653.37 602 Ac-LTF$r8GlaYWAQL$AAAAAa-NH₂ 510 1973.03 983 1974.04 987.52 658.68 603 Ac-LTF$r8F4gYWAQL$AAAAAa-NH₂ 511 2004.1 937.86 2005.11 1003.06 669.04 604 Ac-LTF$r82mRYWAQL$AAAAAa-NH₂ 512 1984.13 958.58 1985.14 993.07 662.38 605 Ac-LTF$r8ipKYWAQL$AAAAAa-NH₂ 513 1970.14 944.52 1971.15 986.08 657.72 606 Ac-LTF$r8F4NH3YWAQLSAAAAAa-NH₂ 514 1962.08 946 1963.09 982.05 655.03 607 Ac-LTF$r8EYWAAL$AAAAAa-NH₂ 515 1872.02 959.32 1873.03 937.02 625.01 608 Ac-LTF$r8EYWALL$AAAAAa-NH₂ 516 1914.07 980.88 1915.08 958.04 639.03 609 Ac-LTF$r8EYWAAibL$AAAAAa-NH₂ 517 1886.03 970.61 1887.04 944.02 629.68 610 Ac-LTF$r8EYWASL$AAAAAa-NH₂ 518 1888.01 980.51 1889.02 945.01 630.34 611 Ac-LTF$r8EYWANL$AAAAAa-NH₂ 519 1915.02 1006.41 1916.03 958.52 639.35 612 Ac-LTF$r8FYWACitL$AAAAAa-NH₂ 520 1958.07 1959.08 980.04 653.7 613 Ac-LTF$r8EYWAHL$AAAAAa-NH₂ 521 1938.04 966.24 1934.05 970.03 647.02 614 Ac-LTF$r8EYWARL$AAAAAa-NH₂ 522 1957.08 1958.09 979.55 653.37 615 Ac-LTF$r8EpYWAQL$AAAAAa-NH₂ 523 2009.01 2010.02 1005.51 670.68 616 Cbm-LTF$r8EYWAQCbaSSAA-NH₂ 524 1590.85 1591.86 796.43 531.29 617 Cbm-LTF$r8EYWAQL$AAAAAa-NH₂ 525 1930.04 1931.05 966.03 644.35 618 Ac-LTF$r8EYWAQL$SAAAAa-NH₂ 526 1445.04 1005.11 1946.05 973.53 649.35 619 Ac-LTF$r8EYAATAQL$AAAASa-NH₂ 527 1945.04 986.52 1946.05 973.53 649.35 620 Ac-LTF$r8EYWAQL$SAAASa-NH₂ 528 1961.03 993.27 1962.04 981.52 654.68 621 Ac-LTF$r8EYWAQTba$AAAAAa-NH₂ 529 1943.06 983.1 1944.07 972.54 648.69 622 Ac-LTF$r8EYWAQAdm$AAAAAa-NH₂ 530 2007.09 990.31 2008.1 1004.55 670.04 623 Ac-LTF$r8EYWAQCha$AAAAAa-NH₂ 531 1969.07 987.17 1970.08 985.54 657.36 624 Ac-LTF$r8EYWAQhCha$AAAAAa-NH₂ 532 1983.09 1026.11 1984.1 992.55 662.04 625 Ac-LTF$r8EYWAQF$AAAAAa-NH₂ 533 1963.02 957.01 1964.03 982.52 655.35 626 Ac-LTF$r8EYWAQhF$AAAAAa-NH₂ 534 1977.04 1087.81 1978.05 989.53 660.02 627 Ac-LTF$r8EYWAQL$AANleAAa-NH₂ 535 1971.09 933.45 1972.1 986.55 658.04 628 Ac-LTF$r8EYWAQAdm$AANleAAa-NH₂ 536 2049.13 1017.97 2050.14 1025.57 684.05 629 4-FBz-BaLTF$r8EYWAQL$AAAAAa-NH₂ 537 2080.08 2081.09 1041.05 694.37 630 4-FBz-BaLTF$r8EYWAQCba$SAA-NH₂ 538 1894.97 1895.98 948.49 632.66 631 Ac-LTF$r5EYWAQL$s8AAAAAa-NH₂ 539 1929.04 1072.68 1930.05 965.53 644.02 632 Ac-LTF$r5EYWAQCba$s8SAA-NH₂ 540 1743.92 1107.79 1744.93 872.97 582.31 633 Ac-LTF$r8EYWAQL$AAhhLAAa-NH₂ 541 1999.12 2000.13 1000.57 667.38 634 Ac-LTF$r8EYWAQL$AAAAAAAa-NH₂ 542 2071.11 2072.12 1036.56 691.38 635 Ac-LTF$r8EYWAQL$AAAAAAAAa-NH₂ 543 2142.15 778.1 2143.16 1072.08 715.06 636 Ac-LTF$r8EYWAQL$AAAAAAAAAa-NH₂ 544 2213.19 870.53 2214.2 1107.6 738.74 637 Ac-LTA$r8EYAAQCba$SAA-NH₂ 545 1552.85 1553.86 777.43 518.62 638 Ac-LTA$r8EYAAQL$AAAAAa-NH₂ 546 1737.97 779.45 1738.98 869.99 580.33 639 Ac-LTF$r8EPmpWAQL$AAAAAa-NH₂ 547 2007.03 779.54 2008.04 1004.52 670.02 640 Ac-LTF$r8EPmpWAQCba$SAA-NH₂ 548 1821.91 838.04 1822.92 911.96 608.31 641 Ac-ATF$r8HYWAQL$S-NH₂ 549 1555.82 867.83 1556.83 778.92 519.61 642 Ac-LTF$r8HAWAQL$S-NH₂ 550 1505.84 877.91 1506.85 753.93 502.95 643 Ac-LTF$r8HYWAQA$S-NH₂ 551 1555.82 852.52 1556.83 778.92 519.61 644 Ac-LTF$r8EYWAQCba$SA-NH₂ 552 1672.89 887.18 1673.9 837.45 558.64 645 Ac-LTF$r8EYWAQL$SAA-NH₂ 553 1731.92 873.32 1732.93 866.97 578.31 646 Ac-LTF$r8HYWAQCba$SAA-NH₂ 554 1751.94 873.05 1752.95 876.98 584.99 647 Ac-LTF$r8SWAQCba$SAA-NH₂ 555 1701.91 844.88 1702.92 851.96 568.31 648 Ac-LTF$r8RYWAQCba$SAA-NH₂ 556 1770.98 865.58 1771.99 886.5 591.33 649 Ac-LTF$r8KYWAQCba$SAA-NH₂ 557 1742.98 936.57 1743.99 872.5 582 650 Ac-LTF$r8QYWAQCba$SAA-NH₂ 558 1742.94 930.93 1743.95 872.48 581.99 651 Ac-LTF$r8EYWAACba$SAA-NH₂ 559 1686.9 1032.45 1687.91 844.46 563.31 652 Ac-LTF$r8EYWAQCba$AAA-NH₂ 560 1727.93 895.46 1728.94 864.97 576.98 653 Ac-LTF$r8EYWAQL$AAAAA-OH 561 1858.99 824.54 1860 930.5 620.67 654 Ac-LTF$r8EYWAQL$AAAA-OH 562 1787.95 894.48 1788.96 894.98 596.99 655 Ac-LTF$r8EYWAQL$AA-OH 563 1645.88 856 1646.89 823.95 549.63 656 Ac-LTF$r8AF4b0H2WAQL$AAAAAa-NH₂ 564 657 Ac-LTF$r8AF4b0H2WAAL$AAAAAa-NH₂ 565 658 Ac-LTF$r8EF4b0H2WAQCba$SAA-NH₂ 566 659 Ac-LTF$r8ApYWAQL$AAAAAa-NH₂ 567 660 Ac-LTF$r8ApYWAAL$AAAAAa-NH₂ 568 661 Ac-LTF$r8EpYWAQCba$SAA-NH₂ 569 662 Ac-LTF$rda6AYWAQL$da5AAAAAa-NH₂ 570 1974.06 934.44 663 Ac-LTF$rda6EYWAQCba$da5SAA-NH₂ 571 1846.95 870.52 869.94 664 Ac-LTF$rda6EYWAQL$da5AAAAAa-NH₂ 572 665 Ac-LTF$ra9EYWAQL$a6AAAAAa-NH₂ 573 936.57 935.51 666 Ac-LTF$ra9EYWAQL$a6AAAAAa-NH₂ 574 667 Ac-LTF$ra9EYWAQCba$a6SAA-NH₂ 575 668 Ac-LTA$ra9EYWAQCba$a6SAA-NH₂ 576 669 5-FAM-BaLTF$ra9EYWAQCba$a6SAA-NH₂ 577 670 5-FAM-BaLTF$r8EYWAQL$AAAAAa-NH₂ 578 2316.11 671 5-FAM-BaLTF$/r8EYWAQMAAAAAa-NH₂ 579 2344.15 672 5-FAM-BaLTA$r8EYWAQL$AAAAAa-NH₂ 580 2240.08 673 5-FAM-BaLTF$r8AYWAQL$AAAAAa-NH₂ 581 2258.11 674 5-FAM-BaATF$r8EYWAQL$AAAAAa-NH₂ 582 2274.07 675 5-FAM-BaLAF$r8EYWAQL$AAAAAa-NH₂ 583 2286.1 676 5-FAM-BaLTF$r8EAWAQL$AAAAAa-NH₂ 584 2224.09 677 5-FAM-BaLTF$r8EYAAQL$AAAAAa-NH₂ 585 2201.07 678 5-FAM-BaLTA$r8EYAAQL$AAAAAa-NH₂ 586 2125.04 679 5-FAM-BaLTF$r8EYWAAL$AAAAAa-NH₂ 587 2259.09 680 5-FAM-BaLTF$r8EYWAQA$AAAAAa-NH₂ 588 2274.07 681 5-FAM-BaLTF$/r8EYWAQCba$/SAA-NH₂ 589 2159.03 682 5-FAM-BaLTA$r8EYWAQCba$SAA-NH₂ 590 2054.97 683 5-FAM-BaLTF$r8EYAAQCba$SAA-NH₂ 591 2015.96 684 5-FAM-BaLTA$r8EYAAQCba$SAA-NH₂ 592 1939.92 685 5-FAM-BaQSQQTF$r8NLWRLL$QN-NH₂ 593 2495.23 686 5-TAMRA-BaLTF$r8EYWAQCba$SAA-NH₂ 594 2186.1 687 5-TAMRA-BaLTA$r8EYWAQCba$SAA-NH₂ 595 2110.07 688 5-TAMRA-BaLTF$r8EYAAQCba$SAA-NH₂ 596 2071.06 689 5-TAMRA-BaLTA$r8EYAAQCba$SAA-NH₂ 597 1995.03 690 5-TAMRA-BaLTF$/r8EYWAQCba$/SAA-NH₂ 598 2214.13 691 5-TAMRA-BaLTF$r8EYWAQL$AAAAAa-NH₂ 599 2371.22 692 5-TAMRA-BaLTA$r8EYWAQL$AAAAAa-NH₂ 600 2295.19 693 5-TAMRA-BaLTF$/r8EYWAQMAAAAAa-NH₂ 601 2399.25 694 Ac-LTF$r8EYWCou7QCba$SAA-OH 602 1947.93 695 Ac-LTF$r8EYWCou7QCba$S-OH 603 1805.86 696 Ac-LTA$r8EYWCou7QCba$SAA-NH₂ 604 1870.91 697 Ac-LTF$r8EYACou7QCba$SAA-NH₂ 605 1831.9 698 Ac-LTA$r8EYACou7QCba$SAA-NH₂ 606 1755.87 699 Ac-LTF$/r8EYWCou7QCba$/SAA-NH₂ 607 1974.98 700 Ac-LTF$r8EYWCou7QL$AAAAAa-NH₂ 608 2132.06 701 Ac-LTF$/r8EYWCou7QL$/AAAAAa-NH₂ 609 2160.09 702 Ac-LTF$r8EYWCou7QL$AAAAA-OH 610 2062.01 703 Ac-LTF$r8EYWCou7QL$AAAA-OH 611 1990.97 704 Ac-LTF$r8EYWCou7QL$AAA-OH 612 1919.94 705 Ac-LTF$r8EYWCou7QL$AA-OH 613 1848.9 706 Ac-LTF$r8EYWCou7QL$A-OH 614 1777.86 707 Ac-LTF$r8EWAQL$AAAASa-NH₂ 615 iso2 974.4 973.53 708 Ac-LTF$r8AYWAAL$AAAAAa-NH₂ 616 iso2 1814.01 908.82 1815.02 908.01 605.68 709 Biotin-BaLTF$r8EYWAQL$AAAAAa-NH₂ 617 2184.14 1093.64 2185.15 1093.08 729.05 710 Ac-LTF$r8HAWAQL$S-NH₂ 618 iso2 1505.84 754.43 1506.85 753.93 502.95 711 Ac-LTF$r8EYWAQCba$SA-NH₂ 619 iso2 1672.89 838.05 1673.9 837.45 558.64 712 Ac-LTF$r8HYWAQCba$SAA-NH₂ 620 iso2 1751.94 877.55 1752.95 876.98 584.99 713 Ac-LTF$r8SYWAQCba$SAA-NH₂ 621 iso2 1701.91 852.48 1702.92 851.96 568.31 714 Ac-LTF$r8RYWAQCba$SAA-NH₂ 622 iso2 1770.98 887.45 1771.99 886.5 591.33 715 Ac-LTF$r8KYWAQCba$SAA-NH₂ 623 iso2 1742.98 872.92 1743.99 872.5 582 716 Ac-LTF$r8EYWAQCba$AAA-NH₂ 624 iso2 1727.93 865.71 1728.94 864.97 576.98 717 Ac-LTF$r8EYWAQL$AAAAAaBaC-NH₂ 625 2103.09 1053.12 2104.1 1052.55 702.04 718 Ac-LTF$r8EYWAQL$AAAAAadPeg4C-NH₂ 626 2279.19 1141.46 2280.2 1140.6 760.74 719 Ac-LTA$r8AYWAAL$AAAAAa-NH₂ 627 1737.98 870.43 1738.99 870 580.33 720 Ac-LTF$r8AYAAAL$AAAAAa-NH₂ 628 1698.97 851 1699.98 850.49 567.33 721 5-FAM-BaLTF$r8AYWAAL$AAAAAa-NH₂ 629 2201.09 1101.87 2202.1 1101.55 734.7 722 Ac-LTA$r8AYWAQL$AAAAAa-NH₂ 630 1795 898.92 1796.01 898.51 599.34 723 Ac-LTF$r8AYAAQL$AAAAAa-NH₂ 631 1755.99 879.49 1757 879 586.34 724 Ac-LTF$rda6AYWAAL$da5AAAAAa-NH₂ 632 1807.97 1808.98 904.99 603.66 725 FITC-BaLTF$r8EYWAQL$AAAAAa-NH₂ 633 2347.1 1174.49 2348.11 1174.56 783.37 726 FITC-BaLTF$r8EYWAQCba$SAA-NH₂ 634 2161.99 1082.35 2163 1082 721.67 733 Ac-LTF$r8EYWAQL$EAAAAa-NH₂ 635 1987.05 995.03 1988.06 994.53 663.36 734 Ac-LTF$r8AYWAQL$EAAAAa-NH₂ 636 1929.04 966.35 1930.05 965.53 644.02 735 Ac-LTF$r8EYWAQL$AAAAAaBaKbio-NH₂ 637 2354.25 1178.47 2355.26 1178.13 785.76 736 Ac-LTF$r8AYWAAL$AAAAAa-NH₂ 638 1814.01 908.45 1815.02 908.01 605.68 737 Ac-LTF$r8AYAAAL$AAAAAa-NH₂ 639 iso2 1698.97 850.91 1699.98 850.49 567.33 738 Ac-LTF$r8AYAAQL$AAAAAa-NH₂ 640 iso2 1755.99 879.4 1757 879 586.34 739 Ac-LTF$r8EYWAQL$EAAAAa-NH₂ 641 iso2 1987.05 995.21 1988.06 994.53 663.36 740 Ac-LTF$r8AYWAQL$EAAAAa-NH₂ 642 iso2 1929.04 966.08 1930.05 965.53 644.02 741 Ac-LTF$r8EYWAQCba$SAAAAa-NH₂ 643 1957.04 980.04 1958.05 979.53 653.35 742 Ac-LTF$r8EYWAQLStAAA$r5AA-NH₂ 644 2023.12 1012.83 2024.13 1012.57 675.38 743 Ac-LTF$r8EYWAQL$A$AAA$A-NH₂ 645 2108.17 1055.44 2109.18 1055.09 703.73 744 Ac-LTF$r8EYWAQL$AA$AAA$A-NH₂ 646 2179.21 1090.77 2180.22 1090.61 727.41 745 Ac-LTF$r8EYWAQL$AAA$AAA$A-NH₂ 647 2250.25 1126.69 2251.26 1126.13 751.09 746 Ac-AAALTF$r8EYWAQL$AAA-OH 648 1930.02 1931.03 966.02 644.35 747 Ac-AAALTF$r8EYWAQL$AAA-NH₂ 649 1929.04 965.85 1930.05 965.53 644.02 748 Ac-AAAALTF$r8EYWAQL$AAA-NH₂ 650 2000.08 1001.4 2001.09 1001.05 667.7 749 Ac-AAAAALTF$r8EYWAQL$AAA-NH₂ 651 2071.11 1037.13 2072.12 1036.56 691.38 750 Ac-AAAAAALTF$r8EYWAQL$AAA-NH₂ 652 2142.15 2143.16 1072.08 715.06 751 Ac-LTF$rda6EYWAQCba$da6SAA-NH₂ 653 iso2 1751.89 877.36 1752.9 876.95 584.97 752 Ac-t$r5wya$r5f4CF3ekllr-NH₂ 654 844.25 753 Ac-tawy$r5nf4CF3e$r5llr-NH₂ 655 837.03 754 Ac-tawya$r5f4CF3ek$r5lr-NH₂ 656 822.97 755 Ac-tawyanf4CF3e$r5llr$r5a-NH₂ 657 908.35 756 Ac-t$s8wyanf4CF3e$r5llr-NH₂ 658 858.03 757 Ac-tawy$s8nf4CF3ekll$r5a-NH₂ 659 879.86 758 Ac-tawya$s8f4CF3ekllr$r5a-NH₂ 660 936.38 759 Ac-tawy$s8naekll$r5a-NH₂ 661 844.25 760 5-FAM-Batawy$s8nf4CF3ekll$r5a-NH₂ 662 761 5-FAM-Batawy$s8naekll$r5a-NH₂ 663 762 Ac-tawy$s8nf4CF3eall$r5a-NH₂ 664 763 Ac-tawy$s8nf4CF3ekll$r5aaaaa-NH₂ 665 764 Ac-tawy$s8nf4CF3eall$r5aaaaa-NH₂ 666

Table 3a shows a selection of peptidomimetic macrocycles.

TABLE 3a SEQ Calc Calc Calc ID Exact Found (M + (M + (M + Sequence NO: Iso Mass Mass 1)/1 2)/2 3)/3 244 Ac-LTF$r8EF4coohWAQCba$SANleA-NH₂ 667 1885 943.59 1886.01 943.51 629.34 331 Ac-LTF$r8EYWAQL$AAAAAa-NH₂ 668 iso2 1929.04 966.08 1930.05 965.53 644.02 555 Ac-LTF$r8EY6clWAQL$AAAAAa-NH₂ 669 1963 983.28 1964.01 982.51 655.34 557 Ac-AAALTF$r8EYWAQL$AAAAAa-NH₂ 670 2142.15 1072.83 2143.16 1072.08 715.06 558 Ac-LTF34F2$r8EYWAQL$AAAAAa-NH₂ 671 1965.02 984.3 1966.03 983.52 656.01 562 Ac-LTF$r8EYWAQL$AAibAAAa-NH₂ 672 1943.06 973.11 1944.07 972.54 648.69 564 Ac-LTF$r8EYWAQL$AAAAibAa-NH₂ 673 1943.06 973.48 1944.07 972.54 648.69 566 Ac-LTF$r8EYWAQL$AAAAAiba-NH₂ 674 iso2 1943.06 973.38 1944.07 972.54 648.69 567 Ac-LTF$r8EYWAQL$AAAAAAib-NH₂ 675 1943.06 973.01 1944.07 972.54 648.69 572 Ac-LTF$r8EYWAQL$AAAAaa-NH₂ 676 1929.04 966.35 1930.05 965.53 644.02 573 Ac-LTF$r8EYWAQL$AAAAAA-NH₂ 677 1929.04 966.35 1930.05 965.53 644.02 578 Ac-LTF$r8EYWAQL$AAAAASar-NH₂ 678 1929.04 966.08 1930.05 965.53 644.02 551 Ac-LTF$r8EYWAQL$AAAAAa-OH 679 iso2 1930.02 965.89 1931.03 966.02  644.35 662 Ac-LTF$rda6AYWAQL$da5AAAAAa-NH₂ 680 1974.06 934.44 933.49 367 5-FAM-BaLTF$r8EYWAQCba$SAA-NH₂ 681 2131 1067.09 2132.01 1066.51 711.34 349 Ac-LTF$r8EF4coohWAQCba$AAAAAa-NH₂ 682 iso2 1969.04 986.06 1970.05 985.53 657.35 347 Ac-LTF$r8EYWAQCba$AAAAAa-NH₂ 683 iso2 1941.04 972.55 1942.05 971.53 648.02

Table 3b shows a further selection of peptidomimetic macrocycles.

TABLE 3b SEQ Calc Calc Calc ID Exact Found (M + (M + (M + SP Sequence NO: Iso Mass Mass 1)/1 2)/2 3)/3 581 Ac-TF$r8EYWAQL$AAAAAa-NH₂ 684 1815.96 929.85 1816.97 908.99 606.33 582 Ac-F$r8EYWAQL$AAAAAa-NH₂ 685 1714.91 930.92 1715.92 858.46 572.64 583 Ac-LVF$r8EYWAQL$AAAAAa- 686 1927.06 895.12 1928.07 964.54 643.36 NH₂ 584 Ac-AAF$r8EYWAQL$AAAAAa- 687 1856.98 859.51 1857.99 929.5 620 NH₂ 585 Ac-LTF$r8EYWAQL$AAAAa-NH₂ 688 1858 824.08 1859.01 930.01 620.34 586 Ac-LTF$r8EYWAQL$AAAa-NH₂ 689 1786.97 788.56 1787.98 894.49 596.66 587 Ac-LTF$r8EYWAQL$AAa-NH₂ 690 1715.93 1138.57 1716.94 858.97 572.98 588 Ac-LTF$r8EYWAQL$Aa-NH₂ 691 1644.89 1144.98 1645.9 823.45 549.3 589 Ac-LTF$r8EYWAQL$a-NH₂ 692 1573.85 1113.71 1574.86 787.93 525.62

In the sequences shown above and elsewhere, the following abbreviations are used: “Nle” represents norleucine, “Aib” represents 2-aminoisobutyric acid, “Ac” represents acetyl, and “Pr” represents propionyl. Amino acids represented as “$” are alpha-Me S5-pentenyl-alanine olefin amino acids connected by an all-carbon crosslinker comprising one double bond Amino acids represented as “$r5” are alpha-Me R5-pentenyl-alanine olefin amino acids connected by an all-carbon comprising one double bond. Amino acids represented as “$s8” are alpha-Me S8-octenyl-alanine olefin amino acids connected by an all-carbon crosslinker comprising one double bond Amino acids represented as “$r8” are alpha-Me R8-octenyl-alanine olefin amino acids connected by an all-carbon crosslinker comprising one double bond. “Ahx” represents an aminocyclohexyl linker. The crosslinkers are linear all-carbon crosslinker comprising eight or eleven carbon atoms between the alpha carbons of each amino acid. Amino acids represented as “$/” are alpha-Me S5-pentenyl-alanine olefin amino acids that are not connected by any crosslinker Amino acids represented as “$/r5” are alpha-Me R5-pentenyl-alanine olefin amino acids that are not connected by any crosslinker. Amino acids represented as “$/s8” are alpha-Me S8-octenyl-alanine olefin amino acids that are not connected by any crosslinker Amino acids represented as “$/r8” are alpha-Me R8-octenyl-alanine olefin amino acids that are not connected by any crosslinker. Amino acids represented as “Amw” are alpha-Me tryptophan amino acids Amino acids represented as “Aml” are alpha-Me leucine amino acids Amino acids represented as “Amf” are alpha-Me phenylalanine amino acids. Amino acids represented as “2ff” are 2-fluoro-phenylalanine amino acids Amino acids represented as “3ff” are 3-fluoro-phenylalanine amino acids Amino acids represented as “St” are amino acids comprising two pentenyl-alanine olefin side chains, each of which is crosslinked to another amino acid as indicated. Amino acids represented as “St//” are amino acids comprising two pentenyl-alanine olefin side chains that are not crosslinked Amino acids represented as “% St” are amino acids comprising two pentenyl-alanine olefin side chains, each of which is crosslinked to another amino acid as indicated via fully saturated hydrocarbon crosslinks. Amino acids represented as “Ba” are beta-alanine. The lower-case character “e” or “z” within the designation of a crosslinked amino acid (e.g. “$er8” or “$zr8”) represents the configuration of the double bond (E or Z, respectively). In other contexts, lower-case letters such as “a” or “f” represent D amino acids (e.g. D-alanine, or D-phenylalanine, respectively) Amino acids designated as “NmW” represent N-methyltryptophan. Amino acids designated as “NmY” represent N-methyltyrosine. Amino acids designated as “NmA” represent N-methylalanine. “Kbio” represents a biotin group attached to the side chain amino group of a lysine residue Amino acids designated as “Sar” represent sarcosine. Amino acids designated as “Cha” represent cyclohexyl alanine Amino acids designated as “Cpg” represent cyclopentyl glycine Amino acids designated as “Chg” represent cyclohexyl glycine. Amino acids designated as “Cba” represent cyclobutyl alanine Amino acids designated as “F4I” represent 4-iodo phenylalanine. “7L” represents N15 isotopic leucine Amino acids designated as “F3Cl” represent 3-chloro phenylalanine. Amino acids designated as “F4cooh” represent 4-carboxy phenylalanine. Amino acids designated as “F34F2” represent 3,4-difluoro phenylalanine Amino acids designated as “6clW” represent 6-chloro tryptophan Amino acids designated as “$rda6” represent alpha-Me R6-hexynyl-alanine alkynyl amino acids, crosslinked via a dialkyne bond to a second alkynyl amino acid. Amino acids designated as “$da5” represent alpha-Me S5-pentynyl-alanine alkynyl amino acids, wherein the alkyne forms one half of a dialkyne bond with a second alkynyl amino acid Amino acids designated as “$ra9” represent alpha-Me R9-nonynyl-alanine alkynyl amino acids, crosslinked via an alkyne metathesis reaction with a second alkynyl amino acid. Amino acids designated as “$a6” represent alpha-Me S6-hexynyl-alanine alkynyl amino acids, crosslinked via an alkyne metathesis reaction with a second alkynyl amino acid. The designation “iso1” or “iso2” indicates that the peptidomimetic macrocycle is a single isomer.

Amino acids designated as “Cit” represent citrulline Amino acids designated as “Cou4”, “Cou6”, “Cou7” and “Cou8”, respectively, represent the following structures:

In some embodiments, a peptidomimetic macrocycle is obtained in more than one isomer, for example due to the configuration of a double bond within the structure of the crosslinker (E vs Z). Such isomers can or cannot be separable by conventional chromatographic methods. In some embodiments, one isomer has improved biological properties relative to the other isomer. In one embodiment, an E crosslinker olefin isomer of a peptidomimetic macrocycle has better solubility, better target affinity, better in vivo or in vitro efficacy, higher helicity, or improved cell permeability relative to its Z counterpart. In another embodiment, a Z crosslinker olefin isomer of a peptidomimetic macrocycle has better solubility, better target affinity, better in vivo or in vitro efficacy, higher helicity, or improved cell permeability relative to its E counterpart.

Table 3c shows exemplary peptidomimetic macrocycle:

TABLE 3c Structure SP154 (SEQ ID NO: 163)

Ac-LTF$er8EYWAQCba$eSAA-NH2 Chemical Formula: C₈₇H₁₂₅N₁₇O₂₁ Exact Mass: 1743.92 Molecular Weight: 1745.02 SP115 (SEQ ID NO: 124)

Ac-LTF$er8AYWAQhL$eSAA-NH2 Chemical Formula: C₈₅H₁₂₅N₁₇O₁₉ Exact Mass: 1687.93 Molecular Weight: 1689.00 SP114 (SEQ ID NO: 123)

Ac-LTF$zr8AYWAQhL$zSAA-NH2 Chemical Formula: C₈₅H₁₂₅N₁₇O₁₉ Exact Mass: 1687.93 Molecular Weight: 1689.00 SP99 (SEQ ID NO: 108)

Ac-LTF$er8AY6clWAQL$eSAA-NH2 Chemical Formula: C₈₄H₁₂₂ClN₁₇O₁₉ Exact Mass: 1707.88 Molecular Weight: 1709.42 SP388 (SEQ ID NO: 397)

Ac-LTF$er8AYAmwAQL$eAANleA-NH2 Chemical Formula: C₉₁H₁₃₆N₁₈O₁₉ Exact Mass: 1785.02 Molecular Weight: 1786.16 SP331 (SEQ ID NO: 340)

Ac-LTF$er8EYWAQL$eAAAAAa-NH2 Chemical Formula: C₉₅H₁₄₀N₂₀O₂₃ Exact Mass: 1929.04 Molecular Weight: 1930.25 SP445 (SEQ ID NO: 454)

Ac-LTF%r8EYWAQL%AAAAAa-NH2 Chemical Formula: C₉₅H₁₄₂N₂₀O₂₃ Exact Mass: 1931.06 Molecular Weight: 1932.26 SP351 (SEQ ID NO: 360)

Ac-LTF$er8EYWSQCba$eAAAAAa-NH2 Chemical Formula: C₉₆H₁₄₀N₂₀O₂₄ Exact Mass: 1957.03 Molecular Weight: 1958.26 SP71 (SEQ ID NO: 80)

Ac-LTF$er8AYWAQL$eAAla-NH2 Chemical Formula: C₉₀H₁₃₄N₁₈O₁₉ Exact Mass: 1771.01 Molecular Weight: 1772.14 SP69 (SEQ ID NO: 78)

Ac-LTF$er8AYWAQL$eAANleA-NH2 Chemical Formula: C₉₀H₁₃₄N₁₈O₁₉ Exact Mass: 1771.01 Molecular Weight: 1772.14 SP7 (SEQ ID NO: 16)

Ac-LTF$r8AYWAQL$SAF-NH2 Chemical Formula: C₉₀H₁₂₇N₁₇O₁₉ Exact Mass: 1749.95 Molecular Weight: 1751.07 SP160 (SEQ ID NO: 169)

Ac-LTF34F2$er8EYWAQhL$eSAA-NH2 Chemical Formula: C₈₇H₁₂₅F₂N₁₇O₂₁ Exact Mass: 1781.92 Molecular Weight: 1783.02 SP315 (SEQ ID NO: 324)

Ac-LTF$er8AYWAQL$eAAAAAa-NH2 Chemical Formula: C₉₃H₁₃₈N₂₀O₂₁ Exact Mass: 1871.03 Molecular Weight: 1872.21 SP249 (SEQ ID NO: 258)

Ac-LTF$er8EF4coohWAQCba$eAA-l-a-NH2 Chemical Formula: C₉₄H₁₃₆N₁₈O₂₂ Exact Mass: 1869.01 Molecular Weight: 1870.19 SP437 (SEQ ID NO: 446 )

Dmaac-LTF$er8AYWAQL$eAAAAAa-NH2 Chemical Formula: C₉₅H₁₄₃N₂₁O₂₁ Exact Mass: 1914.08 Molecular Weight: 1915.28 SP349 (SEQ ID NO: 358)

Ac-LTF$er8EF4coohWAQCba$eAAAAAa-NH2 Chemical Formula: C₉₇H₁₄₀N₂₀O₂₄ Exact Mass: 1969.03 Molecular Weight: 1970.27 SP555 (SEQ ID NO: 464)

Ac-LTF$er8EY6clWAQL$eAAAAAa-NH2 Chemical Formula: C₉₅H₁₃₉ClN₂₀O₂₃ Exact Mass: 1963.00 Molecular Weight: 1964.69 SP557 (SEQ ID NO: 466)

Ac-AAALTF$er8EYWAQL$eAAAAAa-NH2 Chemical Formula: C₁₀₄H₁₅₅N₂₃O₂₆ Exact Mass: 2142.15 Molecular Weight: 2143.48 SP558 (SEQ ID NO: 467)

Ac-LTF34F2$er8EYWAQL$eAAAAAa-NH2 Chemical Formula: C₉₅H₁₃₈F₂N₂₀O₂₃ Exact Mass: 1965.02 Molecular Weight: 1966.23 SP367 (SEQ ID NO: 376)

5-FAM-BaLTF$er8EYWAQCba$eSAA-NH2 SP562 (SEQ ID NO: 471)

Ac-LTF$er8EYWAQL$eAAibAAAa-NH2 Chemical Formula: C₉₆H₁₄₂N₂₀O₂₃ Exact Mass: 1943.06 Molecular Weight: 1944.27 SP564 (SEQ ID NO: 473)

Ac-LTF$er8EYWAQL$eAAAAibAa-NH2 Chemical Formula: C₉₆H₁₄₂N₂₀O₂₃ Exact Mass: 1943.06 Molecular Weight: 1944.27 SP566 (SEQ ID NO: 475)

SP567 (SEQ ID NO: 476)

Ac-LTF$er8EYWAQL$eAAAAAAib-NH2 Chemical Formula: C₉₆H₁₄₂N₂₀O₂₃ Exact Mass: 1943.06 Molecular Weight: 1944.27 SP572 (SEQ ID NO: 481)

Ac-LTF$er8EYWAQL$eAAAAaa-NH2 Chemical Formula: C₉₅H₁₄₀N₂₀O₂₃ Exact Mass: 1929.04 Molecular Weight: 1930.25 SP573 (SEQ ID NO: 482)

Ac-LTF$er8EYWAQL$eAAAAAA-NH2 Chemical Formula: C₉₅H₁₄₀N₂₀O₂₃ Exact Mass: 1929.04 Molecular Weight: 1930.25 SP578 (SEQ ID NO: 487)

Ac-LTF$er8EYWAQL$eAAAAASar-NH2 Chemical Formula: C₉₅H₁₄₀N₂₀O₂₃ Exact Mass: 1929.04 Molecular Weight: 1930.25 SP664 (SEQ ID NO: 572)

Ac-LTF$rda6EYWAQL$da5AAAAAa-NH₂ Chemical Formula: C₉₅H₁₃₄N₂₀O₂₃ Exact Mass: 1922.99 Molecular Weight: 1924.20 SP664 (SEQ ID NO: 572)

Ac-LTF$rda6EYWAQL$da5AAAAAa-NH2 Chemical Formula: C₉₅H₁₃₄N₂₀O₂₃ Exact Mass: 1922.99 Molecular Weight: 1924.20 (SEQ ID NO: 1500)

Chemical Formula: C₉₆H₁₃₆N₂₀O₂₃ Exact Mass: 1937.01 Molecular Weight: 1938.23

In some embodiments, peptidomimetic macrocycles exclude peptidomimetic macrocycles shown in Table 4a:

TABLE 4a Number Sequence SEQ ID NO: 765 L$r5QETFSD$s8WKLLPEN 693 766 LSQ$r5TFSDLW$s8LLPEN 694 767 LSOE$r5FSDLWK$s8LPEN 695 768 LSQET$r5SDLWKL$s8PEN 696 769 LSQETF$r5DLWKLL$s8EN 697 770 LXQETFS$r5LWKLLP$s8N 698 771 LSQETFSD$r5WKLLPE$s8 699 772 LSQQTF$r5DLWKLL$s8EN 700 773 LSQETF$r5DLWKLL$s8QN 701 774 LSQQTF$r5DLWKLL$s8QN 702 775 LSQETF$r5NLWKLL$s8QN 703 776 LSQQTF$r5NLWKLL$s8QN 704 777 LSQQTF$r5NLWRLL$s8QN 705 778 QSQQTF$r5NLWKLL$s8QN 706 779 QSQQTF$r5NLWRLL$s8QN 707 780 QSQQTA$r5NLWRLL$s8QN 708 781 L$r8QETFSD$WKLLPEN 709 782 LSQ$r8TFSDLW$LLPEN 710 783 LSQE$r8FSDLWK$LPEN 711 784 LSQET$r8SDLWKL$PEN 712 785 LSQETF$r8DLWKLL$EN 713 786 LXQETFS$r8LWKLLP$N 714 787 LSQETFSD$r8WKLLPE$ 715 788 LSQQTF$r8DLWKLL$EN 716 789 LSQETF$r8DLWKLL$QN 717 790 LSQQTF$r8DLWKLL$QN 718 791 LSQETF$r8NLWKLL$QN 719 792 LSQQTF$r8NLWKLL$QN 720 793 LSQQTF$r8NLWRLL$QN 721 794 QSQQTF$r8NLWKLL$QN 722 795 QSQQTF$r8NLWRLL$QN 723 796 QSQQTA$r8NLWRLL$QN 724 797 QSQQTF$r8NLWRKK$QN 725 798 QQTF$r8DLWRLL$EN 726 799 QQTF$r8DLWRLL$ 727 800 LSQQTF$DLW$LL 728 801 QQTF$DLW$LL 729 802 QQTA$r8DLWRLL$EN 730 803 QSQQTF$r5NLWRLL$s8QN 731 (dihydroxylated olefin) 804 QSQQTA$r5NLWRLL$s8QN 732 (dihydroxylated olefin) 805 QSQQTF$r8DLWRLL$QN 733 806 QTF$r8NLWRLL$ 734 807 QSQQTF$NLW$LLPQN 735 808 QS$QTF$NLWRLLPQN 736 809 $TFS$LWKLL 737 810 ETF$DLW$LL 738 811 QTF$NLW$LL 739 812 $SQE$FSNLWKLL 740 In Table 4a, X represents S or any amino acid. Peptides shown can comprise an N-terminal capping group such as acetyl or an additional linker such as beta-alanine between the capping group and the start of the peptide sequence.

In some embodiments, peptidomimetic macrocycles do not comprise a peptidomimetic macrocycle structure as shown in Table 4a.

In other embodiments, peptidomimetic macrocycles exclude peptidomimetic macrocycles shown in Table 4b.

TABLE 4b SEQ Observed ID Exact mass SP# Sequence NO: Mass M + 2 (m/e)  813 Ac-LSQETF$r8DLWKLL$EN-NH₂  741 2068.13 1035.07 1035.36  814 Ac-LSQETF$r8NLWKLL$QN-NH₂  742 2066.16 1034.08 1034.31  815 Ac-LSQQTF$r8NLWRLL$QN-NH₂  743 2093.18 1047.59 1047.73  816 Ac-QSQQTF$r8NLWKLL$QN-NH₂  744 2080.15 1041.08 1041.31  817 Ac-QSQQTF$r8NLWRLL$QN-NH₂  745 2108.15 1055.08 1055.32  818 Ac-QSQQTA$r8NLWRLL$QN-NH₂  746 2032.12 1017.06 1017.24  819 Ac-QAibQQTF$r8NLWRLL$QN-NH₂  747 2106.17 1054.09 1054.34  820 Ac-QSQQTFSNLWRLLPQN-NH₂  748 2000.02 1001.01 1001.26  821 Ac-QSQQTF$/r8NLWRLL$/QN-NH₂  749 2136.18 1069.09 1069.37  822 Ac-QSQAibTF$r8NLWRLL$QN-NH₂  750 2065.15 1033.58 1033.71  823 Ac-QSQQTF$r8NLWRLL$AN-NH₂  751 2051.13 1026.57 1026.70  824 Ac-ASQQTFSr8NLWRLL$QN-NH₂  752 2051.13 1026.57 1026.90  825 Ac-QSQQTF$r8ALWRLL$QN-NH₂  753 2065.15 1033.58 1033.41  826 Ac-QSQETF$r8NLWRLL$QN-NH₂  754 2109.14 1055.57 1055.70  827 Ac-RSQQTFSr8NLWRLL$QN-NH₂  755 2136.20 1069.10 1069.17  828 Ac-RSQQTF$r8NLWRLL$EN-NH₂  756 2137.18 1069.59 1069.75  829 Ac-LSQETFSDLWKLLPEN-NH₂  757 1959.99  981.00 981.24  830 Ac-QSQ$TFSSLWRLLPQN-NH₂  758 2008.09 1005.05 1004.97  831 Ac-QSQQ$FSNSWRLLPQN-NH₂  759 2036.06 1019.03 1018.86  832 Ac-QSQQT$SNL$RLLPQN-NH₂  760 1917.04  959.52 959.32  833 Ac-QSQQTF$NLW$LLPQN-NH₂  761 2007.06 1004.53 1004.97  834 Ac-RTQATF$r8NQWAibANle$TNAibTR-NH₂  762 2310.26 1156.13 1156.52  835 Ac-QSQQTF$r8NLWRLL$RN-NH₂  763 2136.20 1069.10 1068.94  836 Ac-QSQRTF$r8NLWRLL$QN-NH₂  764 2136.20 1069.10 1068.94  837 Ac-QSQQTF$r8NNleWRLL$QN-NH₂  765 2108.15 1055.08 1055.44  838 Ac-QSQQTF$r8NLWRNleL$QN-NH₂  766 2108.15 1055.08 1055.84  839 Ac-QSQQTF$r8NLWRLNle$QN-NH₂  767 2108.15 1055.08 1055.12  840 Ac-QSQQTY$r8NLWRLL$QN-NH₂  768 2124.15 1063.08 1062.92  841 Ac-RAibQQTF$r8NLWRLL$QN-NH₂  769 2134.22 1068.11 1068.65  842 Ac-MPRFMDYWEGLN-NH₂  770 1598.70  800.35 800.45  843 Ac-RSQQRF$r8NLWRLL$QN-NH₂  771 2191.25 1096.63 1096.83  844 Ac-QSQQRF$r8NLWRLL$QN-NH₂  772 2163.21 1082.61 1082.87  845 Ac-RAibQQRF$r8NLWRLL$QN-NH₂  773 2189.27 1095.64 1096.37  846 Ac-RSQQRF$r8NFWRLL$QN-NH₂  774 2225.23 1113.62 1114.37  847 Ac-RSQQRF4r8NYWRLL$QN-NH₂  775 2241.23 1121.62 1122.37  848 Ac-RSQQTF$r8NLWQLL$QN-NH₂  776 2108.15 1055.08 1055.29  849 Ac-QSQQTF$r8NLWQAmlL$QN-NH₂  777 2094.13 1048.07 1048.32  850 Ac-QSQQTF$r8NAmlWRLL$QN-NH₂  778 2122.17 1062.09 1062.35  851 Ac-NlePRF$r8DYWEGL$QN-NH₂  779 1869.98  935.99 936.20  852 Ac-NlePRF$r8NYWRLL$QN-NH₂  780 1952.12  977.06 977.35  853 Ac-RF$r8NLWRLL$Q-NH₂  781 1577.96  789.98 790.18  854 Ac-QSQQTF$r8N2ffWRLL$QN-NH₂  782 2160.13 1081.07 1081.40  855 Ac-QSQQTF$r8N3ffWRLL$QN-NH₂  783 2160.13 1081.07 1081.34  856 Ac-QSQQTF#r8NLWRLL#QN-NH₂  784 2080.12 1041.06 1041.34  857 Ac-RSQQTA$r8NLWRLL$QN-NH₂  785 2060.16 1031.08 1031.38  858 Ac-QSQQTF%r8NLWRLL%QN-NH₂  786 2110.17 1056.09 1056.55  859 HepQSQ$TFSNLWRLLPQN-NH₂  787 2051.10 1026.55 1026.82  860 HepQSQ$TF$r8NLWRLL$QN-NH₂  788 2159.23 1080.62 1080.89  861 Ac-QSQQTF$r8NL6clWRLL$QN-NH₂  789 2142.11 1072.06 1072.35  862 Ac-QSQQTF$r8NLMe6clwRLL$QN-NH₂  790 2156.13 1079.07 1079.27  863 Ac-LTFEHYWAQLTS-NH₂  791 1535.74  768.87 768.91  864 Ac-LTF$HYW$QLTS-NH₂  792 1585.83  793.92 794.17  865 Ac-LTFE$YWASLTS-NH₂  793 1520.79  761.40 761.67  866 Ac-LTF$zr8HYWAQL$zS-NH₂  794 1597.87  799.94 800.06  867 Ac-LTF$r8HYWRQL$S-NH₂  795 1682.93  842.47 842.72  868 Ac-QS$QTFStNLWRLL$s8QN-NH₂  796 2145.21 1073.61 1073.90  869 Ac-QSQQTASNLWRLLPQN-NH₂  797 1923.99  963.00 963.26  870 Ac-QSQQTA$/r8NLWRLLS/QN-NH₂  798 2060.15 1031.08 1031.24  871 Ac-ASQQTF$/r8NLWRLLS/QN-NH₂  799 2079.16 1040.58 1040.89  872 Ac-$SQQ$FSNLWRLLAibQN-NH₂  800 2009.09 1005.55 1005.86  873 Ac-QS$QTF$NLWRLLAibQN-NH₂  801 2023.10 1012.55 1012.79  874 Ac-QSQQ$FSN$WRLLAibQN-NH₂  802 2024.06 1013.03 1013.31  875 Ac-QSQQTF$NLW$LLAibQN-NH₂  803 1995.06  998.53 998.87  876 Ac-QSQQTFS$LWRSLAibQN-NH₂  804 2011.06 1006.53 1006.83  877 Ac-QSQQTFSNLW$LLASN-NH₂  805 1940.02  971.01 971.29  878 Ac-$/SQQ$/FSNLWRLLAibQN-NH₂  806 2037.12 1019.56 1019.78  879 Ac-QS$/QTF$/NLWRLLAibQN-NH₂  807 2051.13 1026.57 1026.90  880 Ac-QSQQ$/FSN$/WRLLAibQN-NH₂  808 2052.09 1027.05 1027.36  881 Ac-QSQQTF$/NLW$/LLAibQN-NH₂  809 2023.09 1012.55 1013.82  882 Ac-QSQ$TFS$LWRLLAibQN-NH₂  810 1996.09  999.05 999.39  883 Ac-QSQ$/TFS$/LWRLLAibQN-NH₂  811 2024.12 1013.06 1013.37  884 Ac-QS$/QTFSt//NLWRLL$/s8QN-NH₂  812 2201.27 1101.64 1102.00  885 Ac-$r8SQQTFS$LWRLLAibQN-NH₂  813 2038.14 1020.07 1020.23  886 Ac-QSQ$r8TFSNLW$LLAibQN-NH₂  814 1996.08  999.04 999.32  887 Ac-QSQQTFS$r8LWRLLA$N-NH₂  815 2024.12 1013.06 1013.37  888 Ac-QS$r5QTFStNLW$LLAibQN-NH₂  816 2032.12 1017.06 1017.39  889 Ac-$/r8SQQTFSS/LWRLLAibQN-NH₂  817 2066.17 1034.09 1034.80  890 Ac-QSQ$/r8TFSNLW$/LLAibQN-NH₂  818 2024.11 1013.06 1014.34  891 Ac-QSQQTFS$/r8LWRLLA$/N-NH₂  819 2052.15 1027.08 1027.16  892 Ac-QS$/r5QTFSt//NLW$/LLAibQN-NH₂  820 2088.18 1045.09 1047.10  893 Ac-QSQQTFSNLWRLLAibQN-NH₂  821 1988.02  995.01 995.31  894 Hep/QSQ$/TF$48NLWRLL$/QN-NH₂  822 2215.29 1108.65 1108.93  895 Ac-ASQQTF$r8NLRWLL$QN-NH₂  823 2051.13 1026.57 1026.90  896 Ac-QSQQTF$/r8NLWRLL$/Q-NH₂  824 2022.14 1012.07 1012.66  897 Ac-QSQQTF$r8NLWRLL$Q-NH₂  825 1994.11  998.06 998.42  898 Ac-AAARAA$r8AAARAA$AA-NH₂  826 1515.90  758.95 759.21  899 Ac-LTFEHYWAQLTSA-NH₂  827 1606.78  804.39 804.59  900 Ac-LTF$r8HYWAQL$SA-NH₂  828 1668.90  835.45 835.67  901 Ac-ASQQTFSNLWRLLPQN-NH₂  829 1943.00  972.50 973.27  902 Ac-QS$QTFStNLW$r5LLAibQN-NH₂  830 2032.12 1017.06 1017.30  903 Ac-QSQQTFAibNLWRLLAibQN-NH₂  831 1986.04  994.02 994.19  904 Ac-QSQQTFNleNLWRLLNleQN-NH₂  832 2042.11 1022.06 1022.23  905 Ac-QSQQTF$/r8NLWRLLAibQN-NH₂  833 2082.14 1042.07 1042.23  906 Ac-QSQQTF$/r8NLWRLLNleQN-NH₂  834 2110.17 1056.09 1056.29  907 Ac-QSQQTFAibNLWRLL$/QN-NH₂  835 2040.09 1021.05 1021.25  908 Ac-QSQQTFNleNLWRLL$/QN-NH₂  836 2068.12 1035.06 1035.31  909 Ac-QSQQTF%r8NL6clWRNleL%QN-NH₂  837 2144.13 1073.07 1073.32  910 Ac-QSQQTF%r8NLMe6clWRLL%QN-NH₂  838 2158.15 1080.08 1080.31  911 Ac-FNle$YWE$L-NH₂  839 1160.63 — 1161.70  912 Ac-F$r8AYWELL$A-NH₂  840 1344.75 — 1345.90  913 Ac-F$r8AYWQLL$A-NH₂  841 1343.76 — 1344.83  914 Ac-NlePRF$r8NYWELL$QN-NH₂  842 1925.06  963.53 963.69  915 Ac-NlePRF$r8DYWRLL$QN-NH₂  843 1953.10  977.55 977.68  916 Ac-NlePRF$r8NYWRLL$Q-NH₂  844 1838.07  920.04 920.18  917 Ac-NlePRF$r8NYWRLL$-NH₂  845 1710.01  856.01 856.13  918 Ac-QSQQTF$r8DLWRLL$QN-NH₂  846 2109.14 1055.57 1055.64  919 Ac-QSQQTF$r8NLWRLL$EN-NH₂  847 2109.14 1055.57 1055.70  920 Ac-QSQQTF$r8NLWRLL$QD-NH₂  848 2109.14 1055.57 1055.64  921 Ac-QSQQTF$r8NLWRLL$S-NH₂  849 1953.08  977.54 977.60  922 Ac-ESQQTF$r8NLWRLL$QN-NH₂  850 2109.14 1055.57 1055.70  923 Ac-LTF$r8NLWRNleL$Q-NH₂  851 1635.99  819.00 819.10  924 Ac-LRF$r8NLWRNleL$Q-NH₂  852 1691.04  846.52 846.68  925 Ac-QSQQTF$r8NWWRNleLSQN-NH₂  853 2181.15 1091.58 1091.64  926 Ac-QSQQTF$r8NLWRNleL$Q-NH₂  854 1994.11  998.06 998.07  927 Ac-QTF$r8NLWRNleL$QN-NH₂  855 1765.00  883.50 883.59  928 Ac-NlePRF$r8NWWRLL$QN-NH₂  856 1975.13  988.57 988.75  929 Ac-NlePRF$r8NWWRLL$A-NH₂  857 1804.07  903.04 903.08  930 Ac-TSFAEYWNLLNH₂  858 1467.70  734.85 734.90  931 Ac-QTF$r8HWWSQL$S-NH₂  859 1651.85  826.93 827.12  932 Ac-FM$YWE$L-NH₂  860 1178.58 — 1179.64  933 Ac-QTFEHWWSQLLS-NH₂  861 1601.76  801.88 801.94  934 Ac-QSQQTF$r8NLAmwRLNle$QN-NH₂  862 2122.17 1062.09 1062.24  935 Ac-FMAibY6clWEAc3cL-NH₂  863 1130.47 — 1131.53  936 Ac-FNle$Y6clWE$L-NH₂  864 1194.59 — 1195.64  937 Ac-F$zr8AY6clWEAc3cL$z-NH₂  865 1277.63   39.82 1278.71  938 Ac-F$r8AY6clWEAc3cL$A-NH₂  866 1348.66 — 1350.72  939 Ac-NlePRF$r8NY6clWRLL$QN-NH₂  867 1986.08  994.04 994.64  940 Ac-AF$r8AAWALA$A-NH₂  868 1223.71 — 1224.71  941 Ac-TF$r8AAWRLA$Q-NH₂  869 1395.80  698.90 399.04  942 Pr-TF$r8AAWRLA$Q-NH₂  870 1409.82  705.91 706.04  943 Ac-QSQQTF%r8NLWRNleL%QN-NH₂  871 2110.17 1056.09 1056.22  944 Ac-LTF%r8HYWAQL%SA-NH₂  872 1670.92  836.46 836.58  945 Ac-NlePRF%r8NYWRLL%QN-NH₂  873 1954.13  978.07 978.19  946 Ac-NlePRF%r8NY6clWRLL%QN-NH₂  874 1988.09  995.05 995.68  947 Ac-LTF%r8HY6clWAQL%S-NH₂  875 1633.84  817.92 817.93  948 Ac-QS%QTF%StNLWRLL%s8QN-NH₂  876 2149.24 1075.62 1075.65  949 Ac-LTF%r8HY6clWRQL%S-NH₂  877 1718.91  860.46 860.54  950 Ac-QSQQTF%r8NL6clWRLL%QN-NH₂  878 2144.13 1073.07 1073.64  951 Ac-%r8SQQTFS%LWRLLAibQN-NH₂  879 2040.15 1021.08 1021.13  952 Ac-LTF%r8HYWAQL%S-NH₂  880 1599.88  800.94 801.09  953 Ac-TSF%r8QYWNLL%P-NH₂  881 1602.88  802.44 802.58  954 Ac-LTFEHYWAQLTS-NH₂  882 1535.74  768.87 769.5  955 Ac-F$er8AY6clWEAc3cL$e-NH₂  883 1277.63  639.82 1278.71  956 Ac-AF$r8AAWALA$A-NH₂  884 1277.63  639.82 1277.84  957 Ac-TF$r8AAWRLA$Q-NH₂  885 1395.80  698.90 699.04  958 Pr-TF$r8AAWRLA$Q-NH₂  886 1409.82  705.91 706.04  959 Ac-LTF$er8HYWAQL$eS-NH₂  887 1597.87  799.94 800.44  960 Ac-CCPGCCBaQSQQTF$r8NLWRLL$QN-NH₂  888 2745.30 1373.65 1372.99  961 Ac-CCPGCCBaQSQQTA$r8NLWRLL$QN-NH₂  889 2669.27 1335.64 1336.09  962 Ac-CCPGCCBaNlePRF$r8NYWRLL$QN-NH₂  890 2589.26 1295.63 1296.2  963 Ac-LTF$/r8HYWAQL$/S-NH₂  891 1625.90  813.95 814.18  964 Ac-F%r8HY6clWRAc3cL%-NH₂  892 1372.72  687.36 687.59  965 Ac-QTF%r8HWWSQL%S-NH₂  893 1653.87  827.94 827.94  966 Ac-LTA$r8HYWRQL$S-NH₂  894 1606.90  804.45 804.66  967 Ac-Q$r8QQTFSN$WRLLAibQN-NH₂  895 2080.12 1041.06  1041.61  968 Ac-QSQQ$r8FSNLWR$LAibQN-NH₂  896 2066.11 1034.06  1034.58  969 Ac-F$r8AYWEAc3cL$A-NH₂  897 1314.70  658.35 1315.88  970 Ac-F$r8AYWEAc3cL$S-NH₂  898 1330.70  666.35 1331.87  971 Ac-F$r8AYWEAc3cL$Q-NH₂  899 1371.72  686.86 1372.72  972 Ac-F$r8AYWEAibL$S-NH₂  900 1332.71  667.36 1334.83  973 Ac-F$r8AYWEAL$S-NH₂  901 1318.70  660.35 1319.73  974 Ac-F$r8AYWEQL$S-NH₂  902 1375.72  688.86 1377.53  975 Ac-F$r8HYWEQL$S-NH₂  903 1441.74  721.87 1443.48  976 Ac-F$r8HYWAQL$S-NH₂  904 1383.73  692.87 1385.38  977 Ac-F$r8HYWAAc3cL$S-NH₂  905 1338.71  670.36 1340.82  978 Ac-F$r8HYWRAc3cL$S-NH₂  906 1423.78  712.89 713.04  979 Ac-F$r8AYWEAc3cL#A-NH₂  907 1300.69  651.35 1302.78  980 Ac-NlePTF%r8NYWRLL%QN-NH₂  908 1899.08  950.54 950.56  981 Ac-TF$r8AAWRAL$Q-NH₂  909 1395.80  698.90 699.13  982 Ac-TSF%r8HYWAQL%S-NH₂  910 1573.83  787.92 787.98  983 Ac-F%r8AY6clWEAc3cL%A-NH₂  911 1350.68  676.34 676.91  984 Ac-LTF$r8HYWAQI$S-NH₂  912 1597.87  799.94 800.07  985 Ac-LTF$r8HYWAQNle$S-NH₂  913 1597.87  799.94 800.07  986 Ac-LTF$r8HYWAQL$A-NH₂  914 1581.87  791.94 792.45  987 Ac-LTF$r8HYWAQL$Abu-NH₂  915 1595.89  798.95 799.03  988 Ac-LTF$r8HYWAbuQL$S-NH₂  916 1611.88  806.94 807.47  989 Ac-LTF$er8AYWAQL$eS-NH₂  917 1531.84  766.92 766.96  990 Ac-LAF$r8HYWAQL$S-NH₂  918 1567.86  784.93 785.49  991 Ac-LAF$r8AYWAQL$S-NH₂  919 1501.83  751.92 752.01  992 Ac-LTF$er8AYWAQL$eA-NH₂  920 1515.85  758.93 758.97  993 Ac-LAF$r8AYWAQL$A-NH₂  921 1485.84  743.92 744.05  994 Ac-LTF$r8NLWANleL$Q-NH₂  922 1550.92  776.46 776.61  995 Ac-LTF$r8NLWANleL$A-NH₂  923 1493.90  747.95 1495.6  996 Ac-LTF$r8ALWANleL$Q-NH₂  924 1507.92  754.96 755  997 Ac-LAF$r8NLWANleL$Q-NH₂  925 1520.91  761.46 761.96  998 Ac-LAF$r8ALWANleL$A-NH₂  926 1420.89  711.45 1421.74  999 Ac-A$r8AYWEAc3cL$A-NH₂  927 1238.67  620.34 1239.65 1000 Ac-F$r8AYWEAc3cL$AA-NH₂  928 1385.74  693.87 1386.64 1001 Ac-F$r8AYWEAc3cL$Abu-NH₂  929 1328.72  665.36 1330.17 1013 Ac-F$r8AYWEAc3cL$Nle-NH₂  930 1356.75  679.38 1358.22 1014 Ac-F$r5AYWEAc3cL$s8A-NH₂  931 1314.70  658.35 1315.51 1015 Ac-F$AYWEAc3cL$r8A-NH₂  932 1314.70  658.35 1315.66 1016 Ac-F$r8AYWEAc3cI$A-NH₂  933 1314.70  658.35 1316.18 1017 Ac-F$r8AYWEAc3cNle$A-NH₂  934 1314.70  658.35 1315.66 1018 Ac-F$r8AYWEAmlL$A-NH₂  935 1358.76  680.38 1360.21 1019 Ac-F$r8AYWENleL$A-NH₂  936 1344.75  673.38 1345.71 1020 Ac-F$r8AYWQAc3cL$A-NH₂  937 1313.72  657.86 1314.7 1021 Ac-F$r8AYWAAc3cL$A-NH₂  938 1256.70  629.35 1257.56 1022 Ac-F$r8AYWAbuAc3cL$A-NH₂  939 1270.71  636.36 1272.14 1023 Ac-F$r8AYWNleAc3cL$A-NH₂  940 1298.74  650.37 1299.67 1024 Ac-F$r8AbuYWEAc3cL$A-NH₂  941 1328.72  665.36 1329.65 1025 Ac-F$r8NleYWEAc3cL$A-NH₂  942 1356.75  679.38 1358.66 1026 5-FAM-BaLTFEHYWAQLTS-NH₂  943 1922.82  962.41 962.87 1027 5-FAM-BaLTF%r8HYWAQL%S-NH₂  944 1986.96  994.48 994.97 1028 Ac-LTF$r8HYWAQhL$S-NH₂  945 1611.88  806.94 807 1029 Ac-LTF$r8HYWAQTle$S-NH₂  946 1597.87  799.94 799.97 1030 Ac-LTF$r8HYWAQAdm$S-NH₂  947 1675.91  838.96 839.09 1031 Ac-LTF$r8HYWAQhCha$S-NH₂  948 1651.91  826.96 826.98 1032 Ac-LTF$r8HYWAQCha$S-NH₂  949 1637.90  819.95 820.02 1033 Ac-LTF$r8HYWAc6cQL$S-NH₂  950 1651.91  826.96 826.98 1034 Ac-LTF$r8HYWAc5cQL$S-NH₂  951 1637.90  819.95 820.02 1035 Ac-LThF$r8HYWAQL$S-NH₂  952 1611.88  806.94 807 1036 Ac-LTIgl$r8HYWAQL$S-NH₂  953 1625.90  813.95 812.99 1037 Ac-LTF$r8HYWAQChg$S-NH₂  954 1623.88  812.94 812.99 1038 Ac-LTF$r8HYWAQF$S-NH₂  955 1631.85  816.93 816.99 1039 Ac-LTF$r8HYWAQIgl$S-NH₂  956 1659.88  830.94 829.94 1040 Ac-LTF$r8HYWAQCba$S-NH₂  957 1609.87  805.94 805.96 1041 Ac-LTF$r8HYWAQCpg$S-NH₂  958 1609.87  805.94 805.96 1042 Ac-LTF$r8HhYWAQL$S-NH₂  959 1611.88  806.94 807 1043 Ac-F$r8AYWEAc3chL$A-NH₂  960 1328.72  665.36 665.43 1044 Ac-F$r8AYWEAc3cTle$A-NH₂  961 1314.70  658.35 1315.62 1045 Ac-F$r8AYWEAc3cAdm$A-NH₂  962 1392.75  697.38 697.47 1046 Ac-F$r8AYWEAc3chCha$A-NH₂  963 1368.75  685.38 685.34 1047 Ac-F$r8AYWEAc3cCha$A-NH₂  964 1354.73  678.37 678.38 1048 Ac-F$r8AYWEAc6cL$A-NH₂  965 1356.75  679.38 679.42 1049 Ac-F$r8AYWEAc5cL$A-NH₂  966 1342.73  672.37 672.46 1050 Ac-hF$r8AYWEAc3cL$A-NH₂  967 1328.72  665.36 665.43 1051 Ac-Igl$r8AYWEAc3cL$A-NH₂  968 1342.73  672.37 671.5 1052 Ac-F$r8AYWEAc3cF$A-NH₂  969 1348.69  675.35 675.35 1053 Ac-F$r8AYWEAc3cIgl$A-NH₂  970 1376.72  689.36 688.37 1054 Ac-F$r8AYWEAc3cCba$A-NH₂  971 1326.70  664.35 664.47 1055 Ac-F$r8AYWEAc3cCpg$A-NH₂  972 1326.70  664.35 664.39 1056 Ac-F$r8AhYWEAc3cL$A-NH₂  973 1328.72  665.36 665.43 1057 Ac-F$r8AYWEAc3cL$Q-NH₂  974 1371.72  686.86 1372.87 1058 Ac-F$r8AYWEAibL$A-NH₂  975 1316.72  659.36 1318.18 1059 Ac-F$r8AYWEAL$A-NH₂  976 1302.70  652.35 1303.75 1060 Ac-LAF$r8AYWAAL$A-NH₂  977 1428.82  715.41 715.49 1061 Ac-LTF$r8HYWAAc3cL$S-NH₂  978 1552.84  777.42 777.5 1062 Ac-NleTF$r8HYWAQL$S-NH₂  979 1597.87  799.94 800.04 1063 Ac-VTF$r8HYWAQL$S-NH₂  980 1583.85  792.93 793.04 1064 Ac-FTF$r8HYWAQL$S-NH₂  981 1631.85  816.93 817.02 1065 Ac-WTF$r8HYWAQL$S-NH₂  982 1670.86  836.43 836.85 1066 Ac-RTF$r8HYWAQL$S-NH₂  983 1640.88  821.44 821.9 1067 Ac-KTF$r8HYWAQL$S-NH₂  984 1612.88  807.44 807.91 1068 Ac-LNleFSr8HYWAQL$S-NH₂  985 1609.90  805.95 806.43 1069 Ac-LVF$r8HYWAQL$S-NH₂  986 1595.89  798.95 798.93 1070 Ac-LFF$r8HYWAQL$S-NH₂  987 1643.89  822.95 823.38 1071 Ac-LWF$r8HYWAQL$S-NH₂  988 1682.90  842.45 842.55 1072 Ac-LRF$r8HYWAQL$S-NH₂  989 1652.92  827.46 827.52 1073 Ac-LKF$r8HYWAQL$S-NH₂  990 1624.91  813.46 813.51 1074 Ac-LTFSr8NleYWAQL$S-NH₂  991 1573.89  787.95 788.05 1075 Ac-LTFSr8VYWAQL$S-NH₂  992 1559.88  780.94 780.98 1076 Ac-LTF$r8FYWAQL$S-NH₂  993 1607.88  804.94 805.32 1077 Ac-LTFSr8WYWAQL$S-NH₂  994 1646.89  824.45 824.86 1078 Ac-LTF$r8RYWAQL$S-NH₂  995 1616.91  809.46 809.51 1079 Ac-LTF$r8KYWAQL$S-NH₂  996 1588.90  795.45 795.48 1080 Ac-LTFSr8HNleWAQL$S-NH₂  997 1547.89  774.95 774.98 1081 Ac-LTF$r8HVWAQL$S-NH₂  998 1533.87  767.94 767.95 1082 Ac-LTF$r8HFWAQL$S-NH₂  999 1581.87  791.94 792.3 1083 Ac-LTFSr8HWWAQL$S-NH₂ 1000 1620.88  811.44 811.54 1084 Ac-LTF$r8HRWAQL$S-NH₂ 1001 1590.90  796.45 796.52 1085 Ac-LTF$r8HKWAQL$S-NH₂ 1002 1562.90  782.45 782.53 1086 Ac-LTF$r8HYWNleQL$S-NH₂ 1003 1639.91  820.96 820.98 1087 Ac-LTF$r8HYWVQL$S-NH₂ 1004 1625.90  813.95 814.03 1088 Ac-LTF$r8HYWFQL$S-NH₂ 1005 1673.90  837.95 838.03 1089 Ac-LTF$r8HYWWQL$S-NH₂ 1006 1712.91  857.46 857.5 1090 Ac-LTF$r8HYWKQL$S-NH₂ 1007 1654.92  828.46 828.49 1091 Ac-LTF$r8HYWANleL$S-NH₂ 1008 1582.89  792.45 792.52 1092 Ac-LTF$r8HYWAVL$S-NH₂ 1009 1568.88  785.44 785.49 1093 Ac-LTF$r8HYWAFL$S-NH₂ 1010 1616.88  809.44 809.47 1094 Ac-LTF$r8HYWAWL$S-NH₂ 1011 1655.89  828.95 829 1095 Ac-LTF$r8HYWARL$S-NH₂ 1012 1625.91  813.96 813.98 1096 Ac-LTF$r8HYWAQL$Nle-NH₂ 1013 1623.92  812.96 813.39 1097 Ac-LTF$r8HYWAQL$V-NH₂ 1014 1609.90  805.95 805.99 1098 Ac-LTF$r8HYWAQL$F-NH₂ 1015 1657.90  829.95 830.26 1099 Ac-LTF$r8HYWAQL$W-NH₂ 1016 1696.91  849.46 849.5 1100 Ac-LTF$r8HYWAQL$R-NH₂ 1017 1666.94  834.47 834.56 1101 Ac-LTF$r8HYWAQL$K-NH₂ 1018 1638.93  820.47 820.49 1102 Ac-Q$r8QQTFSN$WRLLAibQN-NH₂ 1019 2080.12 1041.06 1041.54 1103 Ac-QSQQ$r8FSNLWR$LAibQN-NH₂ 1020 2066.11 1034.06 1034.58 1104 Ac-LT2Pal$r8HYWAQL$S-NH₂ 1021 1598.86  800.43 800.49 1105 Ac-LT3Pal$r8HYWAQL$S-NH₂ 1022 1598.86  800.43 800.49 1106 Ac-LT4Pal$r8HYWAQL$S-NH₂ 1023 1598.86  800.43 800.49 1107 Ac-LTF2CF3$r8HYWAQL$S-NH₂ 1024 1665.85  833.93 834.01 1108 Ac-LTF2CNSr8HYWAQL$S-NH₂ 1025 1622.86  812.43 812.47 1109 Ac-LTF2Me$r8HYWAQL$S-NH₂ 1026 1611.88  806.94 807 1110 Ac-LTF3Cl$Sr8HYWAQL$S-NH₂ 1027 1631.83  816.92 816.99 1111 Ac-LTF4CF3$r8HYWAQL$S-NH₂ 1028 1665.85  833.93 833.94 1113 Ac-LTF4tBu$r8HYWAQL$S-NH₂ 1029 1653.93  827.97 828.02 1114 Ac-LTF5F$r8HYWAQL$S-NH₂ 1030 1687.82  844.91 844.96 1115 Ac-LTF$r8HY3BthAAQL$S-NH₂ 1031 1614.83  808.42 808.48 1116 Ac-LTF2Br$r8HYWAQL$S-NH₂ 1032 1675.78  838.89 838.97 1117 Ac-LTF4Br$r8HYWAQL$S-NH₂ 1033 1675.78  838.89 839.86 1118 Ac-LTF2Cl$r8HYWAQL$S-NH₂ 1034 1631.83  816.92 816.99 1119 Ac-LTF4Cl$r8HYWAQL$S-NH₂ 1035 1631.83  816.92 817.36 1120 Ac-LTF3CN$r8HYWAQL$S-NH₂ 1036 1622.86  812.43 812.47 1121 Ac-LTF4CN$r8HYWAQL$S-NH₂ 1037 1622.86  812.43 812.47 1122 Ac-LTF34Cl2$r8HYWAQL$S-NH₂ 1038 1665.79  833.90 833.94 1123 Ac-LTF34F2$r8HYWAQL$S-NH₂ 1039 1633.85  817.93 817.95 1124 Ac-LTF35F2$r8HYWAQL$S-NH₂ 1040 1633.85  817.93 817.95 1125 Ac-LTDip$r8HYWAQL$S-NH₂ 1041 1673.90  837.95 838.01 1126 Ac-LTF2F$r8HYWAQL$S-NH₂ 1042 1615.86  808.93 809 1127 Ac-LTF3F$r8HYWAQL$S-NH₂ 1043 1615.86  808.93 809 1128 Ac-LTF4F$r8HYWAQL$S-NH₂ 1044 1615.86  808.93 809 1129 Ac-LTF4I$r8HYWAQL$S-NH₂ 1045 1723.76  862.88 862.94 1130 Ac-LTF3Me$r8HYWAQL$S-NH₂ 1046 1611.88  806.94 807.07 1131 Ac-LTF4Me$r8HYWAQL$S-NH₂ 1047 1611.88  806.94 807 1132 Ac-LT1Nal$r8HYWAQL$S-NH₂ 1048 1647.88  824.94 824.98 1133 Ac-LT2Nal$r8HYWAQL$S-NH₂ 1049 1647.88  824.94 825.06 1134 Ac-LTF3CF3$r8HYWAQL$S-NH₂ 1050 1665.85  833.93 834.01 1135 Ac-LTF4NO2$r8HYWAQL$S-NH₂ 1051 1642.85  822.43 822.46 1136 Ac-LTF3NO2$r8HYWAQL$S-NH₂ 1052 1642.85  822.43 822.46 1137 Ac-LTF$r82ThiYWAQL$S-NH₂ 1053 1613.83  807.92 807.96 1138 Ac-LTF$r8HBipWAQL$S-NH₂ 1054 1657.90  829.95 830.01 1139 Ac-LTF$r8HF4tBuWAQL$S-NH₂ 1055 1637.93  819.97 820.02 1140 Ac-LTF$r8HF4CF3WAQL$S-NH₂ 1056 1649.86  825.93 826.02 1141 Ac-LTF$r8HF4C1WAQL$S-NH₂ 1057 1615.83  808.92 809.37 1142 Ac-LTF$r8HF4MeWAQL$S-NH₂ 1058 1595.89  798.95 799.01 1143 Ac-LTF$r8HF4BrWAQL$S-NH₂ 1059 1659.78  830.89 830.98 1144 Ac-LTF$r8HF4CNWAQL$S-NH₂ 1060 1606.87  804.44 804.56 1145 Ac-LTF$r8HF4NO2WAQL$S-NH₂ 1061 1626.86  814.43 814.55 1146 Ac-LTF$r8H1NalWAQL$S-NH₂ 1062 1631.89  816.95 817.06 1147 Ac-LTF$r8H2NalWAQL$S-NH₂ 1063 1631.89  816.95 816.99 1148 Ac-LTF$r8HWAQL$S-NH₂ 1064 1434.80  718.40 718.49 1149 Ac-LTF$r8HY1NalAQL$S-NH₂ 1065 1608.87  805.44 805.52 1150 Ac-LTF$r8HY2NalAQL$S-NH₂ 1066 1608.87  805.44 805.52 1151 Ac-LTF$r8HYWAQI$S-NH₂ 1067 1597.87  799.94 800.07 1152 Ac-LTF$r8HYWAQNle$S-NH₂ 1068 1597.87  799.94 800.44 1153 Ac-LTF$er8HYWAQL$eA-NH₂ 1069 1581.87  791.94 791.98 1154 Ac-LTF$r8HYWAQL$Abu-NH₂ 1070 1595.89  798.95 799.03 1155 Ac-LTF$r8HYWAbuQL$S-NH₂ 1071 1611.88  806.94 804.47 1156 Ac-LAF$r8HYWAQL$S-NH₂ 1072 1567.86  784.93 785.49 1157 Ac-LTF$r8NLWANleL$Q-NH₂ 1073 1550.92  776.46 777.5 1158 Ac-LTF$r8ALWANleL$Q-NH₂ 1074 1507.92  754.96 755.52 1159 Ac-LAF$r8NLWANleL$Q-NH₂ 1075 1520.91  761.46 762.48 1160 Ac-F$r8AYWAAc3cL$A-NH₂ 1076 1256.70  629.35 1257.56 1161 Ac-LTF$r8AYWAAL$S-NH₂ 1077 1474.82  738.41 738.55 1162 Ac-LVF$r8AYWAQL$S-NH₂ 1078 1529.87  765.94 766 1163 Ac-LTF$r8AYWAbuQL$S-NH₂ 1079 1545.86  773.93 773.92 1164 Ac-LTF$r8AYWNleQL$S-NH₂ 1080 1573.89  787.95 788.17 1165 Ac-LTF$r8AbuYWAQL$S-NH₂ 1081 1545.86  773.93 773.99 1166 Ac-LTF$r8AYWHQL$S-NH₂ 1082 1597.87  799.94 799.97 1167 Ac-LTF$r8AYWKQL$S-NH₂ 1083 1588.90  795.45 795.53 1168 Ac-LTF$r8AYWOQL$S-NH₂ 1084 1574.89  788.45 788.5 1169 Ac-LTF$r8AYWRQL$S-NH₂ 1085 1616.91  809.46 809.51 1170 Ac-LTF$r8AYWSQL$S-NH₂ 1086 1547.84  774.92 774.96 1171 Ac-LTF$r8AYWRAL$S-NH₂ 1087 1559.89  780.95 780.95 1172 Ac-LTF$r8AYWRQL$A-NH₂ 1088 1600.91  801.46 801.52 1173 Ac-LTF$r8AYWRAL$A-NH₂ 1089 1543.89  772.95 773.03 1174 Ac-LTF$r5HYWAQL$s8S-NH₂ 1090 1597.87  799.94 799.97 1175 Ac-LTF$HYWAQL$r8S-NH₂ 1091 1597.87  799.94 799.97 1176 Ac-LTF$r8HYWAAL$S-NH₂ 1092 1540.84  771.42 771.48 1177 Ac-LTF$r8HYWAAbuL$S-NH₂ 1093 1554.86  778.43 778.51 1178 Ac-LTF$r8HYWALL$S-NH₂ 1094 1582.89  792.45 792.49 1179 Ac-F$r8AYWHAL$A-NH₂ 1095 1310.72  656.36 656.4 1180 Ac-F$r8AYWAAL$A-NH₂ 1096 1244.70  623.35 1245.61 1181 Ac-F$r8AYWSAL$A-NH₂ 1097 1260.69  631.35 1261.6 1182 Ac-F$r8AYWRAL$A-NH₂ 1098 1329.76  665.88 1330.72 1183 Ac-F$r8AYWKAL$A-NH₂ 1099 1301.75  651.88 1302.67 1184 Ac-F$r8AYWOAL$A-NH₂ 1100 1287.74  644.87 1289.13 1185 Ac-F$r8VYWEAc3cL$A-NH₂ 1101 1342.73  672.37 1343.67 1186 Ac-F$r8FYWEAc3cL$A-NH₂ 1102 1390.73  696.37 1392.14 1187 Ac-F$r8WYWEAc3cL$A-NH₂ 1103 1429.74  715.87 1431.44 1188 Ac-F$r8RYWEAc3cL$A-NH₂ 1104 1399.77  700.89 700.95 1189 Ac-F$r8KYWEAc3cL$A-NH₂ 1105 1371.76  686.88 686.97 1190 Ac-F$r8ANleWEAc3cL$A-NH₂ 1106 1264.72  633.36 1265.59 1191 Ac-F$r8AVWEAc3cL$A-NH₂ 1107 1250.71  626.36 1252.2 1192 Ac-F$r8AFWEAc3cL$A-NH₂ 1108 1298.71  650.36 1299.64 1193 Ac-F$r8AWWEAc3cL$A-NH₂ 1109 1337.72  669.86 1338.64 1194 Ac-F$r8ARWEAc3cL$A-NH₂ 1110 1307.74  654.87 655 1195 Ac-F$r8AKWEAc3cL$A-NH₂ 1111 1279.73  640.87 641.01 1196 Ac-F$r8AYWVAc3cL$A-NH₂ 1112 1284.73  643.37 643.38 1197 Ac-F$r8AYWFAc3cL$A-NH₂ 1113 1332.73  667.37 667.43 1198 Ac-F$r8AYWWAc3cL$A-NH₂ 1114 1371.74  686.87 686.97 1199 Ac-F$r8AYWRAc3cL$A-NH₂ 1115 1341.76  671.88 671.94 1200 Ac-F$r8AYWKAc3cL$A-NH₂ 1116 1313.75  657.88 657.88 1201 Ac-F$r8AYWEVL$A-NH₂ 1117 1330.73  666.37 666.47 1202 Ac-F$r8AYWEFL$A-NH₂ 1118 1378.73  690.37 690.44 1203 Ac-F$r8AYWEWL$A-NH₂ 1119 1417.74  709.87 709.91 1204 Ac-F$r8AYWERL$A-NH₂ 1120 1387.77  694.89 1388.66 1205 Ac-F$r8AYWEKL$A-NH₂ 1121 1359.76  680.88 1361.21 1206 Ac-F$r8AYWEAc3cL$V-NH₂ 1122 1342.73  672.37 1343.59 1207 Ac-F$r8AYWEAc3cL$F-NH₂ 1123 1390.73  696.37 1392.58 1208 Ac-F$r8AYWEAc3cL$W-NH₂ 1124 1429.74  715.87 1431.29 1209 Ac-F$r8AYWEAc3cL$R-NH₂ 1125 1399.77  700.89 700.95 1210 Ac-F$r8AYWEAc3cL$K-NH₂ 1126 1371.76  686.88 686.97 1211 Ac-F$r8AYWEAc3cL$AV-NH₂ 1127 1413.77  707.89 707.91 1212 Ac-F$r8AYWEAc3cL$AF-NH₂ 1128 1461.77  731.89 731.96 1213 Ac-F$r8AYWEAc3cL$AW-NH₂ 1129 1500.78  751.39 751.5 1214 Ac-F$r8AYWEAc3cL$AR-NH₂ 1130 1470.80  736.40 736.47 1215 Ac-F$r8AYWEAc3cL$AK-NH₂ 1131 1442.80  722.40 722.41 1216 Ac-F$r8AYWEAc3cL$AH-NH₂ 1132 1451.76  726.88 726.93 1217 Ac-LTF2NO2$r8HYWAQL$S-NH₂ 1133 1642.85  822.43 822.54 1218 Ac-LTA$r8HYAAQL$S-NH₂ 1134 1406.79  704.40 704.5 1219 Ac-LTF$r8HYAAQL$S-NH₂ 1135 1482.82  742.41 742.47 1220 Ac-QSQQTF$r8NLWALL$AN-NH₂ 1136 1966.07  984.04 984.38 1221 Ac-QAibQQTF$r8NLWALL$AN-NH₂ 1137 1964.09  983.05 983.42 1222 Ac-QAibQQTF$r8ALWALL$AN-NH₂ 1138 1921.08  961.54 961.59 1223 Ac-AAAATF$r8AAWAAL$AA-NH₂ 1139 1608.90  805.45 805.52 1224 Ac-F$r8AAWRAL$Q-NH₂ 1140 1294.76  648.38 648.48 1225 Ac-TF$r8AAWAAL$Q-NH₂ 1141 1310.74  656.37 1311.62 1226 Ac-TF$r8AAWRAL$A-NH₂ 1142 1338.78  670.39 670.46 1227 Ac-VF$r8AAWRAL$Q-NH₂ 1143 1393.82  697.91 697.99 1228 Ac-AF$r8AAWAAL$A-NH₂ 1144 1223.71  612.86 1224.67 1229 Ac-TF$r8AAWKAL$Q-NH₂ 1145 1367.80  684.90 684.97 1230 Ac-TF$r8AAWOAL$Q-NH₂ 1146 1353.78  677.89 678.01 1231 Ac-TF$r8AAWSAL$Q-NH₂ 1147 1326.73  664.37 664.47 1232 Ac-LTF$r8AAWRAL$Q-NH₂ 1148 1508.89  755.45 755.49 1233 Ac-F$r8AYWAQL$A-NH₂ 1149 1301.72  651.86 651.96 1234 Ac-F$r8AWWAAL$A-NH₂ 1150 1267.71  634.86 634.87 1235 Ac-F$r8AWWAQL$A-NH₂ 1151 1324.73  663.37 663.43 1236 Ac-F$r8AYWEAL$-NH₂ 1152 1231.66  616.83 1232.93 1237 Ac-F$r8AYWAAL$-NH₂ 1153 1173.66  587.83 1175.09 1238 Ac-F$r8AYWKAL$-NH₂ 1154 1230.72  616.36 616.44 1239 Ac-F$r8AYWOAL$-NH₂ 1155 1216.70  609.35 609.48 1240 Ac-F$r8AYWQAL$-NH₂ 1156 1230.68  616.34 616.44 1241 Ac-F$r8AYWAQL$-NH₂ 1157 1230.68  616.34 616.37 1242 Ac-F$r8HYWDQL$S-NH₂ 1158 1427.72  714.86 714.86 1243 Ac-F$r8HFWEQL$S-NH₂ 1159 1425.74  713.87 713.98 1244 Ac-F$r8AYWHQL$S-NH₂ 1160 1383.73  692.87 692.96 1245 Ac-F$r8AYWKQL$S-NH₂ 1161 1374.77  688.39 688.45 1246 Ac-F$r8AYWOQL$S-NH₂ 1162 1360.75  681.38 681.49 1247 Ac-F$r8HYWSQL$S-NH₂ 1163 1399.73  700.87 700.95 1248 Ac-F$r8HWWEQL$S-NH₂ 1164 1464.76  733.38 733.44 1249 Ac-F$r8HWWAQL$S-NH₂ 1165 1406.75  704.38 704.43 1250 Ac-F$r8AWWHQL$S-NH₂ 1166 1406.75  704.38 704.43 1251 Ac-F$r8AWWKQL$S-NH₂ 1167 1397.79  699.90 699.92 1252 Ac-F$r8AWWOQL$S-NH₂ 1168 1383.77  692.89 692.96 1253 Ac-F$r8HWWSQL$S-NH₂ 1169 1422.75  712.38 712.42 1254 Ac-LTF$r8NYWANleL$Q-NH₂ 1170 1600.90  801.45 801.52 1255 Ac-LTF$r8NLWAQL$Q-NH₂ 1171 1565.90  783.95 784.06 1256 Ac-LTF$r8NYWANleL$A-NH₂ 1172 1543.88  772.94 773.03 1257 Ac-LTF$r8NLWAQL$A-NH₂ 1173 1508.88  755.44 755.49 1258 Ac-LTF$r8AYWANleL$Q-NH₂ 1174 1557.90  779.95 780.06 1259 Ac-LTF$r8ALWAQL$Q-NH₂ 1175 1522.89  762.45 762.45 1260 Ac-LAF$r8NYWANleL$Q-NH₂ 1176 1570.89  786.45 786.5 1261 Ac-LAF$r8NLWAQL$Q-NH₂ 1177 1535.89  768.95 769.03 1262 Ac-LAF$r8AYWANleL$A-NH₂ 1178 1470.86  736.43 736.47 1263 Ac-LAF$r8ALWAQL$A-NH₂ 1179 1435.86  718.93 719.01 1264 Ac-LAF$r8AYWAAL$A-NH₂ 1180 1428.82  715.41 715.41 1265 Ac-F$r8AYWEAc3cLSAAib-NH₂ 1181 1399.75  700.88 700.95 1266 Ac-F$r8AYWAQL$AA-NH₂ 1182 1372.75  687.38 687.78 1267 Ac-F$r8AYWAAc3cL$AA-NH₂ 1183 1327.73  664.87 664.84 1268 Ac-FSr8AYWSAc3cL$AA-NH₂ 1184 1343.73  672.87 672.9 1269 Ac-F$r8AYWEAc3cL$AS-NH₂ 1185 1401.73  701.87 701.84 1270 Ac-F$r8AYWEAc3cL$AT-NH₂ 1186 1415.75  708.88 708.87 1271 Ac-F$r8AYWEAc3cL$AL-NH₂ 1187 1427.79  714.90 714.94 1272 Ac-F$r8AYWEAc3cL$AQ-NH₂ 1188 1442.76  722.38 722.41 1273 Ac-F$r8AFWEAc3cL$AA-NH₂ 1189 1369.74  685.87 685.93 1274 Ac-F$r8AWWEAc3cL$AA-NH₂ 1190 1408.75  705.38 705.39 1275 Ac-F$r8AYWEAc3cL$SA-NH₂ 1191 1401.73  701.87 701.99 1276 Ac-F$r8AYWEAL$AA-NH₂ 1192 1373.74  687.87 687.93 1277 Ac-F$r8AYWENleL$AA-NH₂ 1193 1415.79  708.90 708.94 1278 Ac-F$r8AYWEAc3cL$AbuA-NH₂ 1194 1399.75  700.88 700.95 1279 Ac-F$r8AYWEAc3cL$NleA-NH₂ 1195 1427.79  714.90 714.86 1280 Ac-F$r8AYWEAibL$NleA-NH₂ 1196 1429.80  715.90 715.97 1281 Ac-F$r8AYWEAL$NleA-NH₂ 1197 1415.79  708.90 708.94 1282 Ac-F$r8AYWENleL$NleA-NH₂ 1198 1457.83  729.92 729.96 1283 Ac-F$r8AYWEAibL$Abu-NH₂ 1199 1330.73  666.37 666.39 1284 Ac-F$r8AYWENleL$Abu-NH₂ 1200 1358.76  680.38 680.39 1285 Ac-F$r8AYWEAL$Abu-NH₂ 1201 1316.72  659.36 659.36 1286 Ac-LTF$r8AFWAQL$S-NH₂ 1202 1515.85  758.93 759.12 1287 Ac-LTF$r8AWWAQL$S-NH₂ 1203 1554.86  778.43 778.51 1288 Ac-LTF$r8AYWAQI$S-NH₂ 1204 1531.84  766.92 766.96 1289 Ac-LTF$r8AYWAQNle$S-NH₂ 1205 1531.84  766.92 766.96 1290 Ac-LTF$r8AYWAQL$SA-NH₂ 1206 1602.88  802.44 802.48 1291 Ac-LTF$r8AWWAQL$A-NH₂ 1207 1538.87  770.44 770.89 1292 Ac-LTF$r8AYWAQI$A-NH₂ 1208 1515.85  758.93 759.42 1293 Ac-LTF$r8AYWAQNle$A-NH₂ 1209 1515.85  758.93 759.42 1294 Ac-LTF$r8AYWAQL$AA-NH₂ 1210 1586.89  794.45 794.94 1295 Ac-LTF$r8HWWAQL$S-NH₂ 1211 1620.88  811.44 811.47 1296 Ac-LTF$r8HRWAQL$S-NH₂ 1212 1590.90  796.45 796.52 1297 Ac-LTF$r8HKWAQL$S-NH₂ 1213 1562.90  782.45 782.53 1298 Ac-LTF$r8HYWAQL$W-NH₂ 1214 1696.91  849.46 849.5 1299 Ac-F$r8AYWAbuAL$A-NH₂ 1215 1258.71  630.36 630.5 1300 Ac-F$r8AbuYWEAL$A-NH₂ 1216 1316.72  659.36 659.51 1301 Ac-NlePRF%r8NYWRLL%QN-NH₂ 1217 1954.13  978.07 978.54 1302 Ac-TSF%r8HYWAQL%S-NH₂ 1218 1573.83  787.92 787.98 1303 Ac-LTF%r8AYWAQL%S-NH₂ 1219 1533.86  767.93 768 1304 Ac-HTF$r8HYWAQL$S-NH₂ 1220 1621.84  811.92 811.96 1305 Ac-LHF$r8HYWAQL$S-NH₂ 1221 1633.88  817.94 818.02 1306 Ac-LTF$r8HHWAQL$S-NH₂ 1222 1571.86  786.93 786.94 1307 Ac-LTF$r8HYWHQL$S-NH₂ 1223 1663.89  832.95 832.38 1308 Ac-LTF$r8HYWAHL$S-NH₂ 1224 1606.87  804.44 804.48 1309 Ac-LTF$r8HYWAQL$H-NH₂ 1225 1647.89  824.95 824.98 1310 Ac-LTF$r8HYWAQL$S-NHPr 1226 1639.91  820.96 820.98 1311 Ac-LTF$r8HYWAQL$S-NHsBu 1227 1653.93  827.97 828.02 1312 Ac-LTF$r8HYWAQL$S-NHiBu 1228 1653.93  827.97 828.02 1313 Ac-LTF$r8HYWAQL$S-NHBn 1229 1687.91  844.96 844.44 1314 Ac-LTF$r8HYWAQL$S-NHPe 1230 1700.92  851.46 851.99 1315 Ac-LTF$r8HYWAQL$S-NHChx 1231 1679.94  840.97 841.04 1316 Ac-ETF$r8AYWAQL$S-NH₂ 1232 1547.80  774.90 774.96 1317 Ac-STF$r8AYWAQL$S-NH₂ 1233 1505.79  753.90 753.94 1318 Ac-LEF$r8AYWAQL$S-NH₂ 1234 1559.84  780.92 781.25 1319 Ac-LSF$r8AYWAQL$S-NH₂ 1235 1517.83  759.92 759.93 1320 Ac-LTF$r8EYWAQL$S-NH₂ 1236 1589.85  795.93 795.97 1321 Ac-LTF$r8SYWAQL$S-NH₂ 1237 1547.84  774.92 774.96 1322 Ac-LTF$r8AYWEQL$S-NH₂ 1238 1589.85  795.93 795.9 1323 Ac-LTF$r8AYWAEL$S-NH₂ 1239 1532.83  767.42 766.96 1324 Ac-LTF$r8AYWASL$S-NH₂ 1240 1490.82  746.41 746.46 1325 Ac-LTF$r8AYWAQL$E-NH₂ 1241 1573.85  787.93 787.98 1326 Ac-LTF2CN$r8HYWAQL$S-NH₂ 1242 1622.86  812.43 812.47 1327 Ac-LTF3Cl$r8HYWAQL$S-NH₂ 1243 1631.83  816.92 816.99 1328 Ac-LTDip$r8HYWAQL$S-NH₂ 1244 1673.90  837.95 838.01 1329 Ac-LTF$r8HYWAQTle$S-NH₂ 1245 1597.87  799.94 800.04 1330 Ac-F$r8AY6clWEAL$A-NH₂ 1246 1336.66  669.33 1338.56 1331 Ac-F$r8AYdl6brWEAL$A-NH₂ 1247 1380.61  691.31 692.2 1332 Ac-F$r8AYdl6fWEAL$A-NH₂ 1248 1320.69  661.35 1321.61 1333 Ac-F$r8AYdl4mWEAL$A-NH₂ 1249 1316.72  659.36 659.36 1334 Ac-F$r8AYdl5clWEAL$A-NH₂ 1250 1336.66  669.33 669.35 1335 Ac-F$r8AYdl7mWEAL$A-NH₂ 1251 1316.72  659.36 659.36 1336 Ac-LTF%r8HYWAQL%A-NH₂ 1252 1583.89  792.95 793.01 1337 Ac-LTF$r8HCouWAQL$S-NH₂ 1253 1679.87  840.94 841.38 1338 Ac-LTFEHCouWAQLTS-NH₂ 1254 1617.75  809.88 809.96 1339 Ac-LTA$r8HCouWAQL$S-NH₂ 1255 1603.84  802.92 803.36 1340 Ac-F$r8AYWEAL$AbuA-NH₂ 1256 1387.75  694.88 694.88 1341 Ac-F$r8AYWEAI$AA-NH₂ 1257 1373.74  687.87 687.93 1342 Ac-F$r8AYWEANle$AA-NH₂ 1258 1373.74  687.87 687.93 1343 Ac-F$r8AYWEAm1L$AA-NH₂ 1259 1429.80  715.90 715.97 1344 Ac-F$r8AYWQAL$AA-NH₂ 1260 1372.75  687.38 687.48 1345 Ac-F$r8AYWAAL$AA-NH₂ 1261 1315.73  658.87 658.92 1346 Ac-F$r8AYWAbuAL$AA-NH₂ 1262 1329.75  665.88 665.95 1347 Ac-F$r8AYWNleAL$AA-NH₂ 1263 1357.78  679.89 679.94 1348 Ac-F$r8AbuYWEAL$AA-NH₂ 1264 1387.75  694.88 694.96 1349 Ac-F$r8NleYWEAL$AA-NH₂ 1265 1415.79  708.90 708.94 1350 Ac-F$r8FYWEAL$AA-NH₂ 1266 1449.77  725.89 725.97 1351 Ac-LTF$r8HYWAQhL$S-NH₂ 1267 1611.88  806.94 807 1352 Ac-LTF$r8HYWAQAdm$S-NH₂ 1268 1675.91  838.96 839.04 1353 Ac-LTF$r8HYWAQIgl$S-NH₂ 1269 1659.88  830.94 829.94 1354 Ac-F$r8AYWAQL$AA-NH₂ 1270 1372.75  687.38 687.48 1355 Ac-LTF$r8ALWAQL$Q-NH₂ 1271 1522.89  762.45 762.52 1356 Ac-F$r8AYWEAL$AA-NH₂ 1272 1373.74  687.87 687.93 1357 Ac-F$r8AYWENleL$AA-NH₂ 1273 1415.79  708.90 708.94 1358 Ac-F$r8AYWEAibL$Abu-NH₂ 1274 1330.73  666.37 666.39 1359 Ac-F$r8AYWENleL$Abu-NH₂ 1275 1358.76  680.38 680.38 1360 Ac-F$r8AYWEAL$Abu-NH₂ 1276 1316.72  659.36 659.36 1361 Ac-F$r8AYWEAc3cL$AbuA-NH₂ 1277 1399.75  700.88 700.95 1362 Ac-F$r8AYWEAc3cL$NleA-NH₂ 1278 1427.79  714.90 715.01 1363 H-LTF$r8AYWAQL$S-NH₂ 1279 1489.83  745.92 745.95 1364 mdPEG3-LTF$r8AYWAQL$S-NH₂ 1280 1679.92  840.96 840.97 1365 mdPEG7-LTF$r8AYWAQL$S-NH₂ 1281 1856.02  929.01 929.03 1366 Ac-F$r8ApmpEt6clWEAL$A-NH₂ 1282 1470.71  736.36 788.17 1367 Ac-LTF3Cl$r8AYWAQL$S-NH₂ 1283 1565.81  783.91 809.18 1368 Ac-LTF3Cl$r8HYWAQL$A-NH₂ 1284 1615.83  808.92 875.24 1369 Ac-LTF3Cl$r8HYWWQL$S-NH₂ 1285 1746.87  874.44 841.65 1370 Ac-LTF3Cl$r8AYWWQL$S-NH₂ 1286 1680.85  841.43 824.63 1371 Ac-LTF$r8AYWWQL$S-NH₂ 1287 1646.89  824.45 849.98 1372 Ac-LTF$r8HYWWQL$A-NH₂ 1288 1696.91  849.46 816.67 1373 Ac-LTF$r8AYWWQL$A-NH₂ 1289 1630.89  816.45 776.15 1374 Ac-LTF4F$r8AYWAQL$S-NH₂ 1290 1549.83  775.92 776.15 1375 Ac-LTF2F$r8AYWAQL$S-NH₂ 1291 1549.83  775.92 776.15 1376 Ac-LTF3FSr8AYWAQL$S-NH₂ 1292 1549.83  775.92 785.12 1377 Ac-LTF34F2$r8AYWAQL$S-NH₂ 1293 1567.83  784.92 785.12 1378 Ac-LTF35F2$r8AYWAQL$S-NH₂ 1294 1567.83  784.92 1338.74 1379 Ac-F3Cl$r8AYWEAL$A-NH₂ 1295 1336.66  669.33 705.28 1380 Ac-F3Cl$r8AYWEAL$AA-NH₂ 1296 1407.70  704.85 680.11 1381 Ac-F$r8AY6clWEAL$AA-NH₂ 1297 1407.70  704.85 736.83 1382 Ac-F$r8AY6clWEAL$-NH₂ 1298 1265.63  633.82 784.1 1383 Ac-LTF$r8HYWAQLSt/S-NH₂ 1299 16.03    9.02 826.98 1384 Ac-LTF$r8HYWAQL$S-NHsBu 1300 1653.93  827.97 828.02 1385 Ac-STF$r8AYWAQL$S-NH₂ 1301 1505.79  753.90 753.94 1386 Ac-LTF$r8AYWAEL$S-NH₂ 1302 1532.83  767.42 767.41 1387 Ac-LTF$r8AYWAQL$E-NH₂ 1303 1573.85  787.93 787.98 1388 mdPEG3-LTF$r8AYWAQL$S-NH₂ 1304 1679.92  840.96 840.97 1389 Ac-LTF$r8AYWAQhL$S-NH₂ 1305 1545.86  773.93 774.31 1390 Ac-LTF$r8AYWAQCha$S-NH₂ 1306 1571.88  786.94 787.3 1391 Ac-LTF$r8AYWAQChg$S-NH₂ 1307 1557.86  779.93 780.4 1392 Ac-LTF$r8AYWAQCba$S-NH₂ 1308 1543.84  772.92 780.13 1393 Ac-LTF$r8AYWAQF$S-NH₂ 1309 1565.83  783.92 784.2 1394 Ac-LTF4F$r8HYWAQhL$S-NH₂ 1310 1629.87  815.94 815.36 1395 Ac-LTF4F$r8HYWAQCha$S-NH₂ 1311 1655.89  828.95 828.39 1396 Ac-LTF4F$r8HYWAQChg$S-NH₂ 1312 1641.87  821.94 821.35 1397 Ac-LTF4F$r8HYWAQCba$S-NH₂ 1313 1627.86  814.93 814.32 1398 Ac-LTF4F$r8AYWAQhL$S-NH₂ 1314 1563.85  782.93 782.36 1399 Ac-LTF4F$r8AYWAQCha$S-NH₂ 1315 1589.87  795.94 795.38 1400 Ac-LTF4F$r8AYWAQChg$S-NH₂ 1316 1575.85  788.93 788.35 1401 Ac-LTF4F$r8AYWAQCba$S-NH₂ 1317 1561.83  781.92 781.39 1402 Ac-LTF3Cl$r8AYWAQhL$S-NH₂ 1318 1579.82  790.91 790.35 1403 Ac-LTF3Cl$r8AYWAQCha$S-NH₂ 1319 1605.84  803.92 803.67 1404 Ac-LTF3Cl$r8AYWAQChg$S-NH₂ 1320 1591.82  796.91 796.34 1405 Ac-LTF3C1$r8AYWAQCba$S-NH₂ 1321 1577.81  789.91 789.39 1406 Ac-LTF$r8AYWAQhF$S-NH₂ 1322 1579.84  790.92 791.14 1407 Ac-LTF$r8AYWAQF3CF3$S-NH₂ 1323 1633.82  817.91 818.15 1408 Ac-LTF$r8AYWAQF3Me$S-NH₂ 1324 1581.86  791.93 791.32 1409 Ac-LTF$r8AYWAQ1Nal$S-NH₂ 1325 1615.84  808.92 809.18 1413 Ac-LTF$r8AYWAQBip$S-NH₂ 1326 1641.86  821.93 822.13 1414 Ac-LTF$r8FYWAQL$A-NH₂ 1327 1591.88  796.94 797.33 1415 Ac-LTF$r8HYWAQL$S-NHAm 1328 1667.94  834.97 835.92 1416 Ac-LTF$r8HYWAQL$S-NHiAm 1329 1667.94  834.97 835.55 1417 Ac-LTF$r8HYWAQL$S-NHnPr3Ph 1330 1715.94  858.97 859.79 1418 Ac-LTF$r8HYWAQL$S-NHnBu3, 3Me 1331 1681.96  841.98 842.49 1419 Ac-LTF$r8HYWAQL$S-NHnPr 1332 1639.91  820.96 821.58 1420 Ac-LTF$r8HYWAQL$S-NHnEt2Ch 1333 1707.98  854.99 855.35 1421 Ac-LTF$r8HYWAQL$S-NHHex 1334 1681.96  841.98 842.4 1422 Ac-LTF$r8AYWAQL$S-NHmdPeg2 1335 1633.91  817.96 818.35 1423 Ac-LTF$r8AYWAQL$A-NHmdPeg2 1336 1617.92  809.96 810.3 1424 Ac-LTF$r8AYWAQL$A-NHmdPeg4 1337 1705.97  853.99 854.33 1425 Ac-F$r8AYdl4mWEAL$A-NH₂ 1338 1316.72  659.36 659.44 1426 Ac-F$r8AYdl5clWEAL$A-NH₂ 1339 1336.66  669.33 669.43 1427 Ac-LThF$r8AYWAQL$S-NH₂ 1340 1545.86  773.93 774.11 1428 Ac-LT2Nal$r8AYWAQL$S-NH₂ 1341 1581.86  791.93 792.43 1429 Ac-LTA$r8AYWAQL$S-NH₂ 1342 1455.81  728.91 729.15 1430 Ac-LTF$r8AYWVQL$S-NH₂ 1343 1559.88  780.94 781.24 1431 Ac-LTF$r8HYWAAL$A-NH₂ 1344 1524.85  763.43 763.86 1432 Ac-LTF$r8VYWAQL$A-NH₂ 1345 1543.88  772.94 773.37 1433 Ac-LTF$r8IYWAQL$S-NH₂ 1346 1573.89  787.95 788.17 1434 Ac-FTF$r8VYWSQL$S-NH₂ 1347 1609.85  805.93 806.22 1435 Ac-ITF$r8FYWAQL$S-NH₂ 1348 1607.88  804.94 805.2 1436 Ac-2NalTF$r8VYWSQL$S-NH₂ 1349 1659.87  830.94 831.2 1437 Ac-ITF$r8LYWSQL$S-NH₂ 1350 1589.89  795.95 796.13 1438 Ac-FTF$r8FYWAQL$S-NH₂ 1351 1641.86  821.93 822.13 1439 Ac-WTFSr8VYWAQL$S-NH₂ 1352 1632.87  817.44 817.69 1440 Ac-WTF$r8WYWAQL$S-NH₂ 1353 1719.88  860.94 861.36 1441 Ac-VTF$r8AYWSQL$S-NH₂ 1354 1533.82  767.91 768.19 1442 Ac-WTF$r8FYWSQL$S-NH₂ 1355 1696.87  849.44 849.7 1443 Ac-FTF$r8IYWAQL$S-NH₂ 1356 1607.88  804.94 805.2 1444 Ac-WTF$r8VYWSQL$S-NH₂ 1357 1648.87  825.44 824.8 1445 Ac-FTF$r8LYWSQL$S-NH₂ 1358 1623.87  812.94 812.8 1446 Ac-YTF$r8FYWSQL$S-NH₂ 1359 1673.85  837.93 837.8 1447 Ac-LTF$r8AY6clWEAL$A-NH₂ 1360 1550.79  776.40 776.14 1448 Ac-LTF$r8AY6clWSQL$S-NH₂ 1361 1581.80  791.90 791.68 1449 Ac-F$r8AY6clWSAL$A-NH₂ 1362 1294.65  648.33 647.67 1450 Ac-FSr8AY6clWQAL$AA-NH₂ 1363 1406.72  704.36 703.84 1451 Ac-LHF$r8AYWAQL$S-NH₂ 1364 1567.86  784.93 785.21 1452 Ac-LTF$r8AYWAQL$S-NH₂ 1365 1531.84  766.92 767.17 1453 Ac-LTF$r8AHWAQL$S-NH₂ 1366 1505.84  753.92 754.13 1454 Ac-LTF$r8AYWAHL$S-NH₂ 1367 1540.84  771.42 771.61 1455 Ac-LTF$r8AYWAQL$H-NH₂ 1368 1581.87  791.94 792.15 1456 H-LTF$r8AYWAQL$A-NH₂ 1369 1473.84  737.92 737.29 1457 Ac-HHF$r8AYWAQL$S-NH₂ 1370 1591.83  796.92 797.35 1458 Ac-aAibWTF$r8VYWSQL$S-NH₂ 1371 1804.96  903.48 903.64 1459 Ac-AibWTF$r8HYWAQL$S-NH₂ 1372 1755.91  878.96 879.4 1460 Ac-AibAWTF$r8HYWAQL$S-NH₂ 1373 1826.95  914.48 914.7 1461 Ac-fWTF$r8HYWAQL$S-NH₂ 1374 1817.93  909.97 910.1 1462 Ac-AibWWTF$r8HYWAQL$S-NH₂ 1375 1941.99  972.00 972.2 1463 Ac-WTF$r8LYWSQL$S-NH₂ 1376 1662.88  832.44 832.8 1464 Ac-WTF$r8NleYWSQL$S-NH₂ 1377 1662.88  832.44 832.6 1465 Ac-LTF$r8AYWSQL$a-NH₂ 1378 1531.84  766.92 767.2 1466 Ac-LTF$r8EYWARL$A-NH₂ 1379 1601.90  801.95 802.1 1467 Ac-LTF$r8EYWAHL$A-NH₂ 1380 1582.86  792.43 792.6 1468 Ac-aTF$r8AYWAQL$S-NH₂ 1381 1489.80  745.90 746.08 1469 Ac-AibTF$r8AYWAQL$S-NH₂ 1382 1503.81  752.91 753.11 1470 Ac-AmfTF$r8AYWAQL$S-NH₂ 1383 1579.84  790.92 791.14 1471 Ac-AmwTF$r8AYWAQL$S-NH₂ 1384 1618.86  810.43 810.66 1472 Ac-NmLTF$r8AYWAQL$S-NH₂ 1385 1545.86  773.93 774.11 1473 Ac-LNmTF$r8AYWAQL$S-NH₂ 1386 1545.86  773.93 774.11 1474 Ac-LSarF$r8AYWAQL$S-NH₂ 1387 1501.83  751.92 752.18 1475 Ac-LGF$r8AYWAQL$S-NH₂ 1388 1487.82  744.91 745.15 1476 Ac-LTNmF$r8AYWAQL$S-NH₂ 1389 1545.86  773.93 774.2 1477 Ac-TF$r8AYWAQL$S-NH₂ 1390 1418.76  710.38 710.64 1478 Ac-ETF$r8AYWAQL$A-NH₂ 1391 1531.81  766.91 767.2 1479 Ac-LTF$r8EYWAQL$A-NH₂ 1392 1573.85  787.93 788.1 1480 Ac-LT2Nal$r8AYWSQL$S-NH₂ 1393 1597.85  799.93 800.4 1481 Ac-LTF$r8AYWAAL$S-NH₂ 1394 1474.82  738.41 738.68 1482 Ac-LTF$r8AYWAQhCha$S-NH₂ 1395 1585.89  793.95 794.19 1483 Ac-LTF$r8AYWAQChg$S-NH₂ 1396 1557.86  779.93 780.97 1484 Ac-LTF$r8AYWAQCba$S-NH₂ 1397 1543.84  772.92 773.19 1485 Ac-LTF$r8AYWAQF3CF3$S-NH₂ 1398 1633.82  817.91 818.15 1486 Ac-LTF$r8AYWAQ1Nal$S-NH₂ 1399 1615.84  808.92 809.18 1487 Ac-LTF$r8AYWAQBip$S-NH₂ 1400 1641.86  821.93 822.32 1488 Ac-LT2Nal$r8AYWAQL$S-NH₂ 1401 1581.86  791.93 792.15 1489 Ac-LTF$r8AYWVQL$S-NH₂ 1402 1559.88  780.94 781.62 1490 Ac-LTF$r8AWWAQL$S-NH₂ 1403 1554.86  778.43 778.65 1491 Ac-FTF$r8VYWSQL$S-NH₂ 1404 1609.85  805.93 806.12 1492 Ac-ITF$r8FYWAQL$S-NH₂ 1405 1607.88  804.94 805.2 1493 Ac-ITF$r8LYWSQL$S-NH₂ 1406 1589.89  795.95 796.22 1494 Ac-FTF$r8FYWAQL$S-NH₂ 1407 1641.86  821.93 822.41 1495 Ac-VTF$r8AYWSQL$S-NH₂ 1408 1533.82  767.91 768.19 1496 Ac-LTF$r8AHWAQL$S-NH₂ 1409 1505.84  753.92 754.31 1497 Ac-LTF$r8AYWAQL$H-NH₂ 1410 1581.87  791.94 791.94 1498 Ac-LTF$r8AYWAHL$S-NH₂ 1411 1540.84  771.42 771.61 1499 Ac-aAibWTF$r8VYWSQL$S-NH₂ 1412 1804.96  903.48 903.9 1500 Ac-AibWTF$r8HYWAQL$S-NH₂ 1413 1755.91  878.96 879.5 1501 Ac-AibAWTF$r8HYWAQL$S-NH₂ 1414 1826.95  914.48 914.7 1502 Ac-fWTF$r8HYWAQL$S-NH₂ 1415 1817.93  909.97 910.2 1503 Ac-AibWWTF$r8HYWAQL$S-NH₂ 1416 1941.99  972.00 972.7 1504 Ac-WTF$r8LYWSQL$S-NH₂ 1417 1662.88  832.44 832.7 1505 Ac-WTF$r8NleYWSQL$S-NH₂ 1418 1662.88  832.44 832.7 1506 Ac-LTF$r8AYWSQL$a-NH₂ 1419 1531.84  766.92 767.2 1507 Ac-LTF$r8EYWARL$A-NH₂ 1420 1601.90  801.95 802.2 1508 Ac-LTF$r8EYWAHL$A-NH₂ 1421 1582.86  792.43 792.6 1509 Ac-aTF$r8AYWAQL$S-NH₂ 1422 1489.80  745.90 746.1 1510 Ac-AibTF$r8AYWAQL$S-NH₂ 1423 1503.81  752.91 753.2 1513 Ac-AmfIT$r8AYWAQL$S-NH₂ 1424 1579.84  790.92 791.2 1514 Ac-AmwTF$r8AYWAQL$S-NH₂ 1425 1618.86  810.43 810.7 1515 Ac-NmLTF$r8AYWAQL$S-NH₂ 1426 1545.86  773.93 774.1 1516 Ac-LNmTF$r8AYWAQL$S-NH₂ 1427 1545.86  773.93 774.4 1517 Ac-LSarF$r8AYWAQL$S-NH₂ 1428 1501.83  751.92 752.1 1518 Ac-TF$r8AYWAQL$S-NH₂ 1429 1418.76  710.38 710.8 1519 Ac-ETF$r8AYWAQL$A-NH₂ 1430 1531.81  766.91 767.4 1520 Ac-LTF$r8EYWAQL$A-NH₂ 1431 1573.85  787.93 788.2 1521 Ac-WTF$r8VYWSQL$S-NH₂ 1432 1648.87  825.44 825.2 1522 Ac-YTF$r8FYWSQL$S-NH₂ 1433 1673.85  837.93 837.3 1523 Ac-F$r8AY6clWSAL$A-NH₂ 1434 1294.65  648.33 647.74 1524 Ac-ETF$r8EYWVQL$S-NH₂ 1435 1633.84  817.92 817.36 1525 Ac-ETF$r8EHWAQL$A-NH₂ 1436 1563.81  782.91 782.36 1526 Ac-ITF$r8EYWAQL$S-NH₂ 1437 1589.85  795.93 795.38 1527 Ac-ITF$r8EHWVQL$A-NH₂ 1438 1575.88  788.94 788.42 1528 Ac-ITF$r8EHWAQL$S-NH₂ 1439 1563.85  782.93 782.43 1529 Ac-LTF4F$r8AYWAQCba$S-NH₂ 1440 1561.83  781.92 781.32 1530 Ac-LTF3Cl$r8AYWAQhL$S-NH₂ 1441 1579.82  790.91 790.64 1531 Ac-LTF3Cl$r8AYWAQCha$S-NH₂ 1442 1605.84  803.92 803.37 1532 Ac-LTF3Cl$r8AYWAQChg$S-NH₂ 1443 1591.82  796.91 796.27 1533 Ac-LTF3Cl$r8AYWAQCba$S-NH₂ 1444 1577.81  789.91 789.83 1534 Ac-LTF$r8AY6clWSQL$S-NH₂ 1445 1581.80  791.90 791.75 1535 Ac-LTF4F$r8HYWAQhL$S-NH₂ 1446 1629.87  815.94 815.36 1536 Ac-LTF4F$r8HYWAQCba$S-NH₂ 1447 1627.86  814.93 814.32 1537 Ac-LTF4F$r8AYWAQhL$S-NH₂ 1448 1563.85  782.93 782.36 1538 Ac-LTF4F$r8AYWAQChg$S-NH₂ 1449 1575.85  788.93 788.35 1539 Ac-ETF$r8EYWVAL$S-NH₂ 1450 1576.82  789.41 788.79 1540 Ac-ETF$r8EHWAAL$A-NH₂ 1451 1506.79  754.40 754.8 1541 Ac-ITF$r8EYWAAL$S-NH₂ 1452 1532.83  767.42 767.75 1542 Ac-ITF$r8EHWVAL$A-NH₂ 1453 1518.86  760.43 760.81 1543 Ac-ITF$r8EHWAAL$S-NH₂ 1454 1506.82  754.41 754.8 1544 Pam-LTF$r8EYWAQL$S-NH₂ 1455 1786.07  894.04 894.48 1545 Pam-ETF$r8EYWAQL$S-NH₂ 1456 1802.03  902.02 902.34 1546 Ac-LTF$r8AYWLQL$S-NH₂ 1457 1573.89  787.95 787.39 1547 Ac-LTF$r8EYWLQL$S-NH₂ 1458 1631.90  816.95 817.33 1548 Ac-LTF$r8EHWLQL$S-NH₂ 1459 1605.89  803.95 804.29 1549 Ac-LTFSr8VYWAQL$S-NH₂ 1460 1559.88  780.94 781.34 1550 Ac-LTF$r8AYWSQL$S-NH₂ 1461 1547.84  774.92 775.33 1551 Ac-ETF$r8AYWAQL$S-NH₂ 1462 1547.80  774.90 775.7 1552 Ac-LTF$r8EYWAQL$S-NH₂ 1463 1589.85  795.93 796.33 1553 Ac-LTF$r8HYWAQL$S-NHAm 1464 1667.94  834.97 835.37 1554 Ac-LTF$r8HYWAQL$S-NHiAm 1465 1667.94  834.97 835.27 1555 Ac-LTF$r8HYWAQL$S-NHnPr3Ph 1466 1715.94  858.97 859.42 1556 Ac-LTF$r8HYWAQL$S-NHnBu3, 3Me 1467 1681.96  841.98 842.67 1557 Ac-LTF$r8HYWAQL$S-NHnBu 1468 1653.93  827.97 828.24 1558 Ac-LTF$r8HYWAQL$S-NHnPr 1469 1639.91  820.96 821.31 1559 Ac-LTF$r8HYWAQL$S-NHnEt2Ch 1470 1707.98  854.99 855.35 1560 Ac-LTF$r8HYWAQL$S-NHHex 1471 1681.96  841.98 842.4 1561 Ac-LTF$r8AYWAQL$S-NHmdPeg2 1472 1633.91  817.96 855.35 1562 Ac-LTF$r8AYWAQL$A-NHmdPeg2 1473 1617.92  809.96 810.58 1563 Ac-LTF$r5AYWAAL$s8S-NH₂ 1474 1474.82  738.41 738.79 1564 Ac-LTF$r8AYWCouQL$S-NH₂ 1475 1705.88  853.94 854.61 1565 Ac-LTF$r8CouYWAQL$S-NH₂ 1476 1705.88  853.94 854.7 1566 Ac-CouTF$r8AYWAQL$S-NH₂ 1477 1663.83  832.92 833.33 1567 H-LTF$r8AYWAQL$A-NH₂ 1478 1473.84  737.92 737.29 1568 Ac-HHF$r8AYWAQL$S-NH₂ 1479 1591.83  796.92 797.72 1569 Ac-LT2Nal$r8AYWSQL$S-NH₂ 1480 1597.85  799.93 800.68 1570 Ac-LTF$r8HCouWAQL$S-NH₂ 1481 1679.87  840.94 841.38 1571 Ac-LTF$r8AYWCou2QL$S-NH₂ 1482 1789.94  895.97 896.51 1572 Ac-LTF$r8Cou2YWAQL$S-NH₂ 1483 1789.94  895.97 896.5 1573 Ac-Cou2TF$r8AYWAQL$S-NH₂ 1484 1747.90  874.95 875.42 1574 Ac-LTF$r8ACou2WAQL$S-NH₂ 1485 1697.92  849.96 850.82 1575 Dmaac-LTF$r8AYWAQL$S-NH₂ 1486 1574.89  788.45 788.82 1576 Hexac-LTF$r8AYWAQL$S-NH₂ 1487 1587.91  794.96 795.11 1577 Napac-LTF$r8AYWAQL$S-NH₂ 1488 1657.89  829.95 830.36 1578 Pam-LTF$r8AYWAQL$S-NH₂ 1489 1728.06  865.03 865.45 1579 Ac-LT2Nal$r8HYAAQL$S-NH₂ 1490 1532.84  767.42 767.61 1580 Ac-LT2Nal$/r8HYWAQL$/S-NH₂ 1491 1675.91  838.96 839.1 1581 Ac-LT2Na$r8HYFAQL$S-NH₂ 1492 1608.87  805.44 805.9 1582 Ac-LT2Nal$r8HWAAQL$S-NH₂ 1493 1555.86  778.93 779.08 1583 Ac-LT2Nal$r8HYAWQL$S-NH₂ 1494 1647.88  824.94 825.04 1584 Ac-LT2Nal$r8HYAAQW$S-NH₂ 1495 1605.83  803.92 804.05 1585 Ac-LTW$r8HYWAQL$S-NH₂ 1496 1636.88  819.44 819.95 1586 Ac-LT1Nal$r8HYWAQL$S-NH₂ 1497 1647.88  824.94 825.41

Observed mass was measured by electrospray ionization-mass spectrometry.

In some embodiments, a peptidomimetic macrocycles disclosed herein do not comprise a peptidomimetic macrocycle structure as shown in Table 4b.

Table 4c shows examples of non-crosslinked polypeptides comprising D-amino acids.

TABLE 4c SEQ ID Exact Found Calc Calc Calc SP Sequence NO: Isomer Mass Mass (M + 1)/1 (M + 2)/2 (M + 3)/3 1587 Ac-tawyanfekllr-NH₂ 1498 777.46 1588 Ac-tawyanf4CF3ekllr-NH₂ 1499 811.41

Example 2 Cell Viability Assay

Cells were thawed from a liquid nitrogen preserved state. Once cells were expanded and divide at their expected doubling times, screening began. Cells were seeded in growth media in black 384-well tissue culture treated plates at 500 cells/well. Cells were equilibrated in assay plates via centrifugation and placed in incubators attached to the Dosing Modules at 37° C. for 24 hr before treatment, resulting in cell densities of approximately 500 cells/plate. At the time of treatment, a set of assay plates (which did not receive treatment) were collected and ATP levels were measured by adding ATPLite (Perkin Elmer). These T-zero (T₀) plates were read using ultra-sensitive luminescence on Envision Plate Readers. Using an automated acoustic dispensing system, assay plates were treated with compound or peptide from a 1000×DMSO stock, achieving a 1:1000 working dilution. Final treatment concentrations in the plates were 0 (vehicle), 0.001, 0.003, 0.01, 0.03, 0.1, 0.3, 1, 3, 10 and 30 μM. The assay plates (4 replicates per treatment) were incubated with compound or peptide for 72 hr. After 72 hr, plates were developed for endpoint analysis using ATPLite. All data points were collected via automated processes; quality controlled; and analyzed using Zalicus proprietary software. Assay plates were accepted if they passed the following quality control standards: relative luciferase values were consistent throughout the entire experiment, Z-factor scores were greater than 0.6, and untreated/vehicle controls behaved consistently on the plate.

Growth Inhibition (GI), used as a measure of cell viability, was measured at the time of dosing (T₀) and after 72 hr (T₇₂). A GI reading of 0% represents no growth inhibition; a GI 100% represents complete growth inhibition, a cytostatic effect. A GI 200% represents complete death of all cells in the culture well. Compounds reaching an activity plateau of GI 200% were considered cytotoxic. GI was calculated by the following test and equation:

${{If}\mspace{14mu} T} < {V_{0}\text{:}\mspace{14mu} 100*\left( {1 - \frac{T - V_{0}}{V_{0}}} \right)}$ ${{If}\mspace{14mu} T} \geq {V_{0}\text{:}\mspace{14mu} 100*\left( {1 - \frac{T - V_{0}}{V - V_{0}}} \right)}$

Where T is the signal measure for a test article, V is the vehicle-treated control measure, and V₀ is the vehicle control measure at time zero. This formula was derived from the Growth Inhibition calculation used in the National Cancer Institute's NCI-60 high throughput screen

Cell lines were assigned as p53 wild-type, mutant, or null from information available from the Cancer Cell Line Encyclopedia. Results for exemplary p53 peptidomimetic macrocycles are shown in Table 5 below

TABLE 5 Cell Viability in p53^(WT)/p53^(MUT) cancer cell lines p53^(WT)/ SP-154 SP-763 Cell lines Cancer Type p53^(MUT) EC₅₀ (μM) EC₅₀ (μM) A2058 skin p53^(MUT) 18.6 30 AsPC-1 Pancreas p53^(MUT) 30 30 Caov-3 ovary p53^(MUT) 12.9 30 Caov-4 ovary p53^(MUT) 30 30 COLO-679 skin p53^(MUT) 13.5 30 COLO-684 endometrium p53^(MUT) 10.1 30 COLO-741 skin p53^(MUT) 18.5 30 EBC-1 Lung-NSCLC p53^(MUT) 30 30 ECC10 gastric p53^(MUT) 15.2 30 KM12 colorectal p53^(MUT) 30 30 LS-123 colorectal p53^(MUT) 30 30 MIA PaCa-2 pancreas p53^(MUT) 30 30 NCI-H508 colorectal p53^(MUT) 30 30 OVCAR-3 ovary p53^(MUT) 30 30 RPMI-7951 skin p53^(MUT) 10.8 30 SF126 brain p53^(MUT) 11 30 SK-OV-3 ovary p53^(MUT) 14.3 30 SW480 colorectal p53^(MUT) 30 30 HCT-116 colorectal p53^(WT) 0.464 1.02 HEC-151 endometrium p53^(WT) 1.19 30 HEC-265 endometrium p53^(WT) 1.78 30 HUH-6-clone5 liver p53^(WT) 0.865 0.791 IST-MES1 lung p53^(WT) 1.43 30 KP-N-RT-BM-1 nerve p53^(WT) 0.285 0.255 KP-N-S19s nerve p53^(WT) 0.176 0.0168 LoVo colorectal p53^(WT) 0.431 0.134 LS-174T colorectal p53^(WT) 0.402 0.205 MSTO-211H lung p53^(WT) 0.288 0.209 MV-4-11 AML p53^(WT) 0.159 0.307 NCI-H929 multiple myeloma p53^(WT) 0.858 0.24 PA-1 ovary p53^(WT) 0.339 0.592 WM-115 skin p53^(WT) 0.425 0.429 COLO-205 colorectal p53^(WT) 0.646 0.429 COLO-849 skin p53^(WT) 1.66 0.501 NCI-H28 lung p53^(WT) 3.42 30

Example 3 Safety and/or Tolerability Study-I Study Objectives

This study was designed to (i) evaluate the safety and/or tolerability of Aileron peptide 1, and to (ii) determine the DLTs and the MTD of the Aileron peptide 1 in patients with advanced solid tumors, including patients with tumors expressing WT p53 protein. Aileron peptide 1 is an alpha helical hydrocarbon cross-linked polypeptide macrocycle, with an amino acid sequence less than 20 amino acids long that is derived from the transactivation domain of wild type human P53 protein and that contains a phenylalanine, a tryptophan and a leucine amino acid in the same positions relative to each other as in the transactivation domain of wild type human P53 protein. Aileron peptide 1 has a single cross link spanning amino acids in the i to the i+7 position of the amino acid sequence and has more than three amino acids between the i+7 position and the carboxyl terminus. Aileron peptide 1 binds to human MDM2 and MDM4 and has an observed mass of 950-975 m/e as measured by electrospray ionization-mass spectrometry.

Investigational Plan Study Design

The study consisted of a Dose Escalation Phase (DEP) and an Expansion Phase (EXP). The DEP was a “3+3” dose escalation design to establish the MTD of Aileron peptide-1. The EXP enrolled patients with specific solid tumors at the MTD to further investigate the clinical safety profile and potential efficacy of the dose level. The selection of patients for the EXP is finalized based on results of the DEP, as well as data from additional nonclinical pharmacology studies. The later includes the investigation of multiple solid cancer cell lines (e.g., breast, bladder, head/neck, gastrointestinal, liver, lung, pancreas, prostate, sarcoma) that facilitates the comparison of cell line sensitivity to Aileron peptide-1 across and within tumor types.

After completing the screening, eligible patients received a single IV dose of Aileron peptide-1 on Days 1, 8, and 15, and remained in the clinic for approximately 8 hours after dosing completion for clinical evaluation, laboratory testing and pharmacokinetic assessments. In addition, a tumor biopsy was performed within 48 hours of Dose 3 (last dose) in Cycle 1 or 2 for pharmacodynamic assessment, unless the biopsy posed a significant risk to the patient. The selection of Cycle 1 or 2 was made at the discretion of the Investigator. Patients returned to the clinic for additional observation and laboratory assessments on Day 22 and for end-of-cycle assessments on Day 29.

Treatment of patients in the dose escalation and the dose expansion phases of the study continued until documentation of disease progression, unacceptable toxicity, or patient or physician decision to discontinue therapy.

p53 Status Determination and Tumor Sampling Requirement Prior to Enrollment:

A central laboratory tested both archived tissue samples or fresh biopsy samples from all patients enrolled in the study for p53 status using Next-Generation Sequencing (NGS).

For the First 3 Dose Levels of Stage 1:

Patients were enrolled irrespective of p53 status. Nevertheless, patients were still tested for p53 status at the central laboratory. To this end, archived tissue was used (sample were not older than 3 years), or alternatively, a fresh biopsy was considered, unless the biopsy posed a significant risk to the patient.

Starting at Dose Level 4 of Stage 1 (and for patients enrolled in Stage 2 of the DEP):

Only patients with tumors expressing WT p53 protein were enrolled. This key inclusion criterion was based on the proposed mechanism of action of Aileron peptide-1, which requires WT p53 protein to be pharmacologically active. The inclusion criterion is also supported by results of in vitro tumor growth assays, in which Aileron peptide-1 demonstrated activity in tumor cells expressing WT p53 protein, but not in cells with null-mutations of p53. Patients met the p53 requirement through one of the following scenarios:

-   -   Patients were eligible based on a previous p53 gene test result         done at a local lab. These patients were still tested for p53         status using NGS at the central laboratory. To this end,         archived tissue was used (sample was not be older than 3 years),         or alternatively, a fresh biopsy was considered, unless the         biopsy posed a significant risk to the patient. Patients who did         not have archived tissue and for whom a biopsy posed a         significant risk, were not enrolled.     -   Patients were eligible based on archived tissue tested for p53         (sample was not be older than 3 years) at the central lab, or         alternatively, a fresh biopsy was considered, unless the biopsy         posed a significant risk to the patient. Patients who didn't         have archived tissue and for whom a biopsy posed a significant         risk, were enrolled.

For patients enrolling into the EXP:

-   -   Only patients with tumors expressing p53 WT were enrolled, and         all patients were tested for p53 status using NGS at the central         laboratory PRIOR to enrollment. Archived tissue were used (if         sample were not older than 1 year), or alternatively, a fresh         biopsy was considered, unless the biopsy posed a significant         risk to the patient. Patients who didn't have archived tissue         and for whom a biopsy posed a significant risk, were not         enrolled.

Only patients with tumors expressing WT p53 protein were enrolled. The determination of p53 status was performed on tumor samples obtained during the screening period. The assay was performed by study sites with required capabilities; otherwise it was performed at a central laboratory. Results from archival tissue samples, if available, could also be used to determine patient eligibility in the DEP. The total number of patients enrolled in the study depended on the number of dose levels and the number of patients in each cohort before MTD is established. Approximately 27 adult patients, exclusive of replacements for patients who discontinue for non-safety reasons, were enrolled in the DEP, and approximately 30 additional patients were enrolled in the EXP. Enrollment of a total of up to 60 patients was planned for the study. Up to 6 clinical sites in the US were planned. The expected accrual phase is approximately 24 months. The expected follow-up phase is approximately 9 months after the last patient is enrolled, for a total study duration of approximately 33 months.

Patients who satisfy all inclusion and exclusion criteria, including documentation of WT p53 status, were enrolled in cohorts of 3 to 6 patients to receive Aileron peptide 1. Aileron peptide 1 was administered by IV infusion over 1 hour (±15 min) on Days 1, 8 and 15 of each 28-day cycle. Treatment continued until disease progression, unacceptable toxicity or patient or physician withdrawal of consent. After the MTD was established, approximately 30 additional patients were enrolled in an expansion cohort to gain further experience at this dose level and in particular patient or tumor types.

Safety was evaluated based on the incidence, severity, duration, causality, seriousness, and type of AE, and changes in the patient's physical examination, vital signs and clinical laboratory results. Investigators used the NCI CTCAE version 4.0 to assess the severity of AEs.

Because the primary objectives of this study were based on safety and pharmacokinetic, statistical analyses were descriptive in nature and accounted for all doses studied and all observed responses, including patients who achieve a complete response (CR) or partial response (PR) or who maintain stable disease (SD) based on RECIST 1.1. Patients who received at least one dose of Aileron peptide 1 constituted the safety population and were be included in all safety analyses. Patients who completed at least one cycle of Aileron peptide 1 and underwent a post-treatment objective disease assessment constituted the efficacy-evaluable patient population.

Patient Population Inclusion Criterias

All patients were required to meet the following inclusion criterias: (i) Male or female patients age 18 years and older, inclusive, at the time of informed consent (ii) Histologically- or cytologically-confirmed malignancy that is metastatic or unresectable and for which standard curative measures do not exist or are no longer effective; (iii) WT p53 status for the relapsing or treatment-refractory solid neoplasm is mandatory for patients enrolling at dose level 4 and higher in Stage 1 of the DEP, as well as for all patients enrolled in Stage 2 of the DEP or in the EXP; (iv) at least one target lesion that is measurable by RECIST 1.1; (v) ECOG performance status 0-1; (vi) predicted life expectancy of ≧3 months; (vii) adequate hematologic function, measured within 7 days prior to the first dose of Aileron peptide 1 (defined as: ANC≧1.5×10⁹/L, Hemoglobin≧9.0 g/d, and Platelets≧100×10⁹/L); (viii) adequate hepatic function, measured within 7 days prior to the first dose of Aileron peptide 1 (defined as: in the absence of disease involvement in the liver:bilirubin≦1.5 times institutional ULN: AST and ALT≦2.5 times ULN; in the presence of disease involvement in the liver:bilirubin≦2 times ULN: AST and ALT≦5 times ULN, (ix) adequate renal function, measured within 7 days prior to the first dose of Aileron peptide 1, (defined as: urinalysis with no evidence of +2 or higher proteinuria, serum creatinine≦1.5 times institutional ULN or calculated creatinine clearance≧50 mL/min (Cockcroft-Gault formula)); (x) acceptable coagulation profile, measured within 7 days prior to the first dose of Aileron peptide 1 (defined as: PT or INR≦1.5 times ULN; aPTT≦1.5 times ULN); (Xi) at least 4 weeks since prior chemotherapy or biologic therapy, radiotherapy or surgery (intra-thoracic, intra-abdominal or intra-pelvic) with recovery to Grade 1 or baseline of significant toxicities, excluding alopecia, from previous therapies. Palliative radiotherapy for bone lesions ≦2 weeks prior to the first dose of Aileron peptide 1 is acceptable if acute toxicity has resolved; (xii) negative serum pregnancy test within 14 days prior to the first dose of Aileron peptide 1 for women of child-bearing potential, defined as a sexually mature woman who has not undergone a hysterectomy or who has not been naturally postmenopausal for ≧24 consecutive months (i.e., who has had menses any time in the preceding 24 consecutive months); (xiii) all patients (males and females) of child-bearing potential agree to use an effective method of birth control (i.e., latex condom, diaphragm, cervical cap, IUD, birth control pill, etc.) beginning two weeks before the first dose of Aileron peptide 1 and for 30 days after the last dose of Aileron peptide 1; (xiv) ability to understand and willingness to sign a written informed consent document; and patients with prostate cancer must continue androgen deprivation therapy, unless such therapy was discontinued 6 months prior to first dose of Aileron peptide 1.

Exclusion Criterias

Patients who meet any of the following criteria at screening or Day-1 were excluded: (i) previous treatment with investigational agents that affect MDM2 or MDMX activity; known hypersensitivity to any study drug component; (iii) known and untreated brain metastases. Patients with brain metastases that have been treated and demonstrated to be clinically stable for ≧30 days can be enrolled onto the dose escalation portion of the study; (iv) history of coagulopathy, platelet disorder or history of non-drug induced thrombocytopenia; (v) history of pulmonary embolism within 6 months prior to the first dose of Aileron peptide 1 or untreated DVT; (vi) required concurrent use of anti-coagulants or anti-platelet medication, with the exception of aspirin doses≦81 mg/day, low-dose SC heparin or SC low-molecular-weight heparin for DVT prophylaxis, or heparin flushes to maintain IV catheter patency; (vii) patients with pre-existing history of or known cardiovascular risk (for example: history of acute coronary syndromes including myocardial infarction, unstable angina, coronary artery bypass graft, angioplasty, or stenting within 6 months prior to the first dose of Aileron peptide 1; uncontrolled hypertension defined as a systolic BP≧160 mmHg and/or diastolic BP≧100 mmHg; pre-existing cardiac failure (New York Heart Association class III-IV); atrial fibrillation on anti-coagulants; clinically significant uncontrolled arrhythmias or arrhythmia requiring treatment, with the exceptions of atrial fibrillation and paroxysmal supraventricular tachycardia; severe valvulopathy; corrected QTc interval on screening ECG≧450 msec for males and ≧470 msec for females); (viii) clinically significant gastrointestinal bleeding within 6 months prior to the first dose of Aileron peptide 1; (ix) clinically significant third-space fluid accumulation (e.g., ascites requiring tapping despite the use of diuretics, or pleural effusion that requires tapping or is associated with shortness of breath); (x) pregnant or lactating females; (xi) evidence of serious and/or unstable pre-existing medical, psychiatric or other condition (including laboratory abnormalities) that could interfere with patient safety or provision of informed consent to participate in this study; (xii) active uncontrolled infection, a history of HIV/AIDS, or a history of hepatitis B or C in the absence of hepatocellular carcinoma. Patients with primary liver cancer that have positive hepatitis serology but are not demonstrating active viral hepatitis can be considered for enrollment if they meet all other inclusion and no other exclusion criteria; (xiii) starting at dose level 4 and higher in Stage 1 of the DEP (as well as for all patients enrolling in Stage 2 of the DEP or in the EXP): Cancers with known Human Papilloma Virus (HPV)-association such as HPV-positive cervical cancers, HPV-positive oropharyngeal cancers or HPV-positive anal cancers; (xiv) known history of another primary malignancy that has not been in remission for ≧2 years. Non-melanoma skin cancer and cervical carcinoma in situ or squamous intraepithelial lesions (e.g., CIN or PIN) are allowed; (xv) any psychological, sociological, or geographical condition that could potentially interfere with compliance with the study protocol and follow-up schedule; (xvi) the required use of any concomitant medications that are predominantly cleared by hepatobiliary transporters (e.g., OATP members OATP1B1 and OATP1B3) within 24 hours of Aileron peptide 1 infusion; (xvii) the use of any investigational agents within 4 weeks or 5 circulating half-lives prior to the first dose of Aileron peptide 1.

Patient Removal/Replacement from Study Therapy

A patient was removed from the study therapy for a variety of reasons, including: (i) disease progression; (ii) unacceptable adverse event(s); (iii) intercurrent illness that prevents further participation; (iv) clinically significant toxicity despite a 2-week dosing delay or after two dose reductions; (v) patient refusal to continue treatment through the study and/or consent withdrawal for study participation; (vi) patient unable or unwilling to comply with study requirements; (vii) pregnancy or failure to use adequate birth control; (viii) general or specific changes in the patient's condition that render the patient unacceptable for further treatment in this study in the judgment of the investigator

Any patient who completed enrollment and did not receive a dose of Aileron peptide 1 was replaced. A patient in the dose escalation portion of the study who discontinued the study prior to completion of the first cycle for reasons other than safety was replaced. A patient in the dose expansion portion of the study who discontinued the study participation prior to the completion of the first cycle of treatment for any reason was replaced.

Treatment Plan Drug Administration Study-1

The study drug was the investigational agent Aileron peptide 1. This investigational agent was be distributed to clinical sites. Patients began treatment with Aileron peptide 1 within 21 days following the start of screening. Aileron peptide 1 drug was be a frozen liquid product supplied in single-use glass vials. The peptidomimetic macrocycle for injection was stored frozen at ≦−15° C. Aileron peptide 1 was introduced into an IV infusion bag containing D5W; known as Aileron peptide 1 dosing solution, and was provided by the site pharmacy for administration to the patient. Aileron peptide 1 dosing solution was labeled with a patient identification number. An investigative staff confirmed this information and its relevancy to the intended patient.

Aileron peptide 1 was administered by IV infusion in D5W over 1 hour (±15 min) on Days 1, 8 and 15 of each 28-day treatment cycle. The pre-defined dose were calculated for each patient based on body weight at the start of each cycle. Aileron peptide 1 was not administered outside of the planned schedule (i.e., infusions on Days 1, 8 and 15 of a 28-day cycle). Deviations if any were noted on the eCRF. Treatment of patients in the dose escalation and the dose expansion phases of the study continued until documentation of disease progression, unacceptable toxicity, or patient or physician decision to discontinue therapy.

In case of infusion-related reactions, Aileron peptide 1 infusion were temporarily discontinued. Pharmacologic agents and other therapeutic interventions were administered per institutional guidelines. The decision to re-start Aileron peptide 1 infusion was made after a careful assessment of the patient.

Starting Dose, Dose Escalation and Dose Reduction Dose Levels for the Dose Escalation Portion of Study

In the Dose Escalation portion of the study, increasing dose levels of Aileron peptide 1 was evaluated in cohorts of 3-6 patients. Aileron peptide 1 was administered by IV infusion over 1 hour (±15 min) on Days 1, 8 and 15 of each 28-day cycle. Patients enrolled in Cohort 1 received Aileron peptide 1 at Dose Level 1 (0.16 mg/kg). Based on allometric scaling, the projected AUC in humans at 0.16 mg/kg (50 μg·hr/mL) is approximately 9% of the rat AUC at STD₁₀ and approximately 6% of the AUC at the monkey HNSTD.

In the absence of DLT, subsequent cohorts of 3 to 6 patients received escalated doses until the MTD was established.

A 2-stage dose escalation design was employed. During the initial Stage 1 Escalation Phase (Table 6), 100% dose increments was utilized until ≧1 of 3 patients in a cohort experiences any Grade≧2 AE that is at least possibly related to study drug. Subsequent dose escalation continued using 3-patient cohorts and the modified Fibonacci sequence (i.e., Stage 2 Escalation Phase; Table 7), until the MTD was established.

TABLE 6 Stage 1 Dose escalation schedule Dose Level Aileron peptide 1 Dose (mg/kg) Level −2 0.04 Level −1 0.08 Level 1 0.16 Level 2 0.32 Level 3 0.64 Level 4 1.25 Level 5 2.5 Level 6 5 Continue 100% dose increase in subsequent cohorts until the MTD is established or Stage 2 escalation schedule is initiated

TABLE 7 Stage 2 Dose escalation Schedule Dose Level Aileron peptide 1 Dose (mg/kg) Level 1 Last Stage 1 Dose × 1.67 Level 2 Previous Dose × 1.5 Level 3 Previous Dose × 1.4 Level 4 Previous Dose × 1.33 In the absence of DLT, continue dose escalation at 33% increments after Stage 2 Level 4 until the MTD is established

The escalation scheme were switched to the Stage 2 Escalation Schedule at any point that the Investigators, Sponsor's Medical Monitor and Safety Physician representative agreed on a more conservative progression.

The observation of DLT(s) was used to make individual patient determinations regarding dose reductions, interruptions or discontinuation throughout the course of the trial, but DLTs occurring during Cycle 1 were used to inform safety and tolerability assessments for dose escalation decisions.

If DLTs was observed in the first cohort, the dose was de-escalated to Dose Level-1. If DLTs were observed at Dose Level-1, the dose was de-escalated to Dose Level-2. If DLTs was observed at Dose Level-2, other dose levels were considered and implemented after discussions among the Investigators, Sponsor's Medical Monitor and Safety Physician representative.

At least three patients were treated at each dose level. If no patients experience a DLT, then the subsequent 3 patients were treated at the next planned dose level.

If DLT was observed in ≧2 of 3 patients in a cohort, then no further dose escalation occurred, and the current dose was defined as the MAD.

If DLT was observed in 1 of 3 patients, then up to 3 additional patients were enrolled at that same dose level. If DLT was observed in ≧2 patients in the expanded cohort, then no further dose escalation will occur, and the current dose was defined as the MAD.

After the MAD was defined, either the previously administered lower dose was expanded to a total of 6 patients, or an intermediate (between the MAD and the next lower dose level) was investigated in up to six patients. The highest dose tolerated without DLT in at least 5 of 6 patients in a cohort was defined as the MTD.

Dose Level for the Expansion Portion of Study

After the MTD was defined, approximately 30 additional patients were enrolled in an expansion study to gain further experience at this dose level and investigate the effect of Aileron peptide 1 in specific patient or tumor types. Two disease types were selected for evaluation, and 15 patients of each disease type were enrolled in each of two cohorts in the expansion study. The dose of Aileron peptide 1 administered to patients in the expansion cohort was derived from evaluation of available safety and other information from patients in the dose escalation portion of the study.

Intra-Patient Dose Escalation

Intra-patient dose escalation was not permitted.

Dose and Schedule Adjustments for Toxicity

Toxicity that occurred during a cycle was required to recover as outlined below for treatment to continue.

Hemoglobin≧8.5 g/dL; ANC≧1.0 10⁹/L; platelet count≧75×10⁹/L; liver function tests back to grade prior to previous cycle (includes PT/INR); other toxicities must return to Grade≦1 or to baseline level if Grade>1 was acceptable for inclusion in the trial.

If a clinically significant AE was observed in a patient during a treatment cycle, further dosing was be delayed until the toxicity has resolved to an acceptable level. Treatment can be delayed by up to 2 weeks to allow for the resolution of AEs, and a dose reduction to the preceding level can be made at the discretion of the Investigator in consultation with Sponsor's Medical Monitor and Safety Physician representative. If a patient experiences multiple AEs, decisions on dosing delay or dose reduction was based on the most severe AE. Any patient who experienced recurrent, clinically significant AE after one dose reduction underwent one additional dose reduction. Patients who continued to experience clinically significant toxicity after a 2-week delay or two dose reductions were discontinued from the study.

Adverse events considered for dose reduction did not include the events assessed by the investigator as exclusively related to underlying disease or other medical condition or concomitant treatment. A patient who experienced an AE considered related to Aileron peptide 1 continued on study if the patient was receiving clinical benefit and/or the Investigator felt continued participation was in the best interest of the patient. In such cases, at the Investigator's discretion and in agreement with Sponsor's Medical Monitor and Safety Physician representative, the dose for a patient was reduced to the preceding lower level.

Up to two dose reductions for a patient were permitted, after which the patient were discontinued from the study.

A patient who experienced a DLT continued treatment at the preceding lower level at the discretion of the Investigator and in agreement with Sponsor's Medical Monitor and Safety Physician representative until disease progression or unacceptable toxicity. Once the dose had been reduced for a patient, it was not re-escalated.

Toxicity grading was based on NCI CTCAE v4.0.

Statistical Methods

Statistical analyses of safety and efficacy for DEP and EXP were primarily descriptive in nature because the objectives of the study were to determine the DLTs and MTD. These objectives were achieved by the results of a deterministic algorithm; thus, statistical hypothesis testing was neither intended nor appropriate within this context. Continuous variables were summarized using descriptive statistics [n, mean, standard deviation, median, minimum, and maximum]. Categorical variables were=e summarized showing the number and percentage (n, %) of patients within each classification.

Study Procedures Schedule of Study Events

The schedule of study activities, including assessments, tests, exams, disease assessments, submission of tissue specimens, and study drug administration) that will be conducted, beginning with screening and continuing through Cycle 1 [day 1, day 8, and day 15 of a 28 day cycle] are outlined in Table 8. Study that will be conducted beginning with Cycle 2 [day 29 of cycle 1=day 1 of cycle 2] are listed on Table 9.

TABLE 8 Schedule of study activities through Cycle 1 Day 29/ Day Day Day 1, 8 ± 15 ± Cycle Clinical Day 1 Day Day 1 d 1 d Day Day 2 ± 3 d Molecular Screen −21 pre- post- 2 ± 3 ± pre- post- pre- post- 16 ± 22 ± Refer to Screen days Day −1 dose dose 4 h 4 h dose dose dose dose 2 d 1 d Table 9 Written informed X X consent Medical history X Demographics X Tumor biopsy or X X archive tissue sample for p53 WT confirmation and biomarker assessment Confirm eligibility X X Blood test for HIV, X hepatitis B and C Serum or urine X pregnancy Vital signs: Blood pressure, X X X X X X X X X X X X pulse, respiration rate, body temperature Physical exam X X X X 12-lead ECG X X X Laboratory assessments: Clinical chemistry X X X X X X X X (glucose, calcium, albumin, total protein, sodium, potassium, CO₂, chloride, BUN [blood urea nitrogen], serum creatinine, ALP, ALT, AST, total and direct bilirubin), hematology (complete blood count, platelets and differential), urinalysis (dipstick measurement [pH, specific gravity, protein, glucose, ketones, nitrite, leukocyte esterase] with microscopic analysis, if results of the dipstick indicate additional testing required), coagulation (PT, INK, aPTT). Collection of blood X for immunogenicity Collection of blood X X X X X X X X X for biomarker assessments Collection of blood X X X X X X X X X for pharmacokinetic assessments ECOG Performance X X X X Status Needle biopsy X X for biomarker assessments Tumor Assessment X Aileron peptide 1 X X X dosing Concomitant X X X X X X X X X X X X medications AE assessment X X X X X X X X X

TABLE 9 Schedule of study activities through Cycle 2 Day 29 of prior cycle/Day 1 of next cycle for Day Day End-of-Study patients continuing 8 ± 15 ± 30 ± 3 d treatment ± 3 d 1 d 1 d Day After even after last dose Pre- post- pre- Post- pre- post- 16 ± numbered or study dose dose dose dose dose dose 2 d cycles withdrawal Serum pregnancy X Vital signs: Blood pressure, pulse, X X X X X X X X respiration rate, body temperature. Physical exam X X X X 12-lead ECG X X X pre-dose At pre- and EOI dose and (+10 min) EOI (+10 min) Laboratory assessments: Clinical chemistry, X X X X X hematology, urinalysis, (Hematology coagulation only) (PT, INR, aPTT). Collection of blood X X X for immunogenicity Collection of blood for X X X X X biomarker assessments (each cycle) Collection of blood X X X X X X for pharmacokinetic assessments (Cycle 2 and End-of-Study only) ECOG Performance X X X X status Needle Biopsy X for biomarker assessments Tumor assessment X X At end of even- numbered cycles. Prior to start of the next treatment cycle Aileron peptide 1 X X X dosing Concomitant X X X X X X X X medications AE assessment X X X X X X X X (begins at the point of the first Aileron peptide 1 infusion and continues until 30 days after last infusion)

Pharmacokinetic Analysis

Levels of Aileron peptide 1 and its metabolites will be measured in blood samples collected at specific time points described below. Pharmacokinetic data will be tabulated and summarized by individual patient and collectively by dose level. Graphical displays will be provided where useful in the interpretation of results.

Blood samples for pharmacokinetic assessment will be collected at the following time points:

TABLE 10 Time points for collection of blood samples for pharmacokinetic assessment Cycle 1 Day 1 within one hour before SOI EOI (+5 min) 30 min after EOI (±5 min) 1 hr after EOI (±5 min) 2 hr after EOI (±10 min) 4 hr after EOI (±10 min) 8 hr after EOI (±10 min) Day 2 24 hours (±4 hr) after the start of Day 1 infusion Day 3 48 hours (±4 hr) after the start of Day 1 infusion Day 8 within one hour before SOI EOI (+5 min) 30 min after EOI (±5 min) 1 hr after EOI (±5 min) 2 hr after EOI (±10 min) 4 hr after EOI (±10 min) Day 15 within one hour before SOI EOI (+5 min) 30 min after EOI (±5 min) 1 hr after EOI (±5 min) 2 hr after EOI (±10 min) 4 hr after EOI (±10 min) 8 hr after EOI (±10 min) Day 16 24 hours (±4 hrs) after the start of Day 15 infusion Cycle 2 Cycle 1 Day 29/ within one hour before SOI Cycle 2 Day 1 EOI (+5 min) 30 min after EOI (±5 min) 1 hr after EOI (±5 min) 2 hr after EOI (±10 min) 4 hr after EOI (±10 min) Day 15 within one hour SOI EOI (±5 min) 30 min after EOI (±5 min) Day 15 (cont.) 1 hr after EOI (±5 min) 2 hr after EOI (±10 min) 4 hr after EOI (±10 min) Day 16 24 hours (±4 hrs) after the start of Day 15 infusion End of study visit During end of study visit

SOI stands for start of infusion of the Aileron peptide 1; EOI stands for the end of infusion of the Aileron peptide 1.

Pharmacodynamic Analysis

Levels of p53, MDM2, MDMX, p21 and caspase will be measured in tumor specimens collected before beginning treatment and at the end of Cycle 1 or Cycle 2. MIC-1 will be measured in blood samples. The specific time points for blood and tissue collection for pharmacodynamic assessments are described below. Pharmacodynamic data will be tabulated and summarized by individual patient and collectively by dose level. Graphical displays will be provided where useful in the interpretation of results.

Results available from previous genetic and biomarker tests, and additional tests of the blood and tumor samples for biomarkers relevant to the safety and efficacy of Aileron peptide-1 can be investigated for possible correlation with patient outcome.

Blood samples for pharmacodynamic assessments will be collected at the following time points:

TABLE 11 Time points for collection of blood samples for pharmacodynamic assessments Cycle 1 Day 1 within 1 hour before the start of infusion (SOI) Day 2 24 hours (±4 hr) after the start of Day 1 infusion Day 3 48 hours (±4 hr) after the start of Day 1 infusion Day 8 within 1 hour before SOI within 1 hour after the end of infusion (EOI) Day 15 within 1 hour before SOI within 1 hour after EOI Day 16 24 hours (±4 hrs) after the start of Day 15 infusion Day 22 During Day 22 visit Each Subsequent Cycle Starting in Cycle 2 Cycle 1 Day 29/ within 1 hour before SOI Cycle 2 Day 1 within 1 hour after EOI Day 15 within 1 hour before SOI Day 16 24 hours (±4 hrs) after the start of Day 15 infusion End of study visit During end of study visit

Assessment of Clinical Activity of the Peptidomimetic Macrocycle

To evaluate clinical activity, response rates and duration of response based on RECIST 1.1 or other appropriate criteria will be provided with a case-by-case description of all patients who exhibit CR, PR or SD. A descriptive analysis of other evidence of anti-tumor activity or other clinical benefit will be provided based on clinical, radiographic or other appropriate assessment of efficacy or clinical anti-tumor activity. Analysis of clinical activity will be conducted on two patient populations: (1) the subset of patients who receive at least one cycle of therapy and have at least one post-baseline disease assessment (the efficacy-evaluable population) and (2) a larger group of patients that includes the efficacy-evaluable population as well as patients who exhibit objective disease progression or experience a DLT and/or unacceptable toxicity prior to the end of Cycle 1.

Imaging scans, physical examination, and/or laboratory-based assays (e.g., prostate specific antigen) for patients with relevant disease indications will be obtained at baseline (within 21 days of Cycle 1 Day 1) and for objective tumor assessment after the second cycle of treatment and after every second treatment cycle thereafter (Cycle 4, Cycle 6, etc.). The same type of imaging, physical examination, or laboratory-based assay procedure will be used for each assessment for a patient. RECIST 1.1 will be used to assess tumor response and duration of response. Scheduled scans (and/or other laboratory-based assay) will be interpreted prior to the start of the next treatment cycle. If the criteria for a CR or PR are met, then the scan will be repeated no earlier than within 4 weeks to confirm the response. A responding patient (CR, PR or SD) will continue on study, with disease assessment after every second cycle, until disease progression, withdrawal of informed consent, or unacceptable toxicity.

Films or other records from imaging procedures, including those procedures performed at a regional or other facility outside of the primary institutions, will be read and reviewed by the radiology staff at the corresponding primary study institution for the patient.

Drug Administration Study-II

Study Objectives

This Phase I open-label, multi-center, dose-escalation, 2-arm study was designed to evaluate the safety, tolerability, pharmacokinetic, pharmacodynamic, and anti-tumor effects of Aileron peptide-1 administered by IV infusion using 2 different dosing regimens of a 28- or 21-day cycle, in patients with advanced solid tumors or lymphomas expressing WT p53 protein (see p53 Status Determination below). Patients received Aileron peptide-1 either once weekly for three consecutive weeks for a 28-day cycle or twice weekly for two consecutive weeks for a 21-day cycle. Many patients with a solid tumor or lymphoma present circulating tumor cells (CTC) in peripheral blood, which can be detected and analyzed using flow cytometry. This enabled the detection of study drug-specific target engagement in these cells.

This study consisted of a DEP and a EXP. The DEP was a “3+3” dose escalation designed to establish the MTD or the OBD of Aileron peptide-1. The EXP enrolled up to 2 distinct groups of patients with specific solid tumors to further investigate the clinical safety profile and potential efficacy of Aileron peptide-1 at the MTD or OBD.

Starting Dose, Dose Escalation, and Dose Reduction

All subjects were dosed at a pre-defined level based on body weight. Starting at Dose Level (DL) 3, patients was sequentially assigned to one of two treatment arms: Dose Regimen (DR) A testing administration of Aileron peptide-1 once per week, or Dose Regimen (DR) B testing administration of Aileron peptide-1 twice per week. For Dose Level 3, DR-A were enrolled first, DR-B were enrolled second. The starting dose (DL-1) in DEP, based on results from nonclinical toxicology assessments, was 0.16 mg/kg.

During the first 2 dose levels, patients received Aileron peptide-1 on Days 1, 8, and 15 of a 28-day cycle. Starting with DL 3, patients in DR-A continued being treated once a week on Days 1, 8, and 15 of a 28-day cycle, whereas patients in DR-B were treated twice a week, on Days 1 and 4, 8 and 11 of a 21-day cycle. This dosing schedule is summarized in FIG. 2.

Doses were doubled in subsequent dose levels until ≧1 of 3 patients in a cohort experienced any drug-related Grade≧2 adverse event (AE). A drug-related AE is an event that is possibly, probably or definitely attributed to Aileron peptide-1. Grading of AEs was defined by the NCI Common Terminology Criteria for Adverse Events (CTCAE) version 4.03. Subsequent dose escalation continued using modified Fibonacci sequence (i.e., 67%, 50%, 40%, and 33%; FIGS. 3 and 4).

Escalation to the next dose level within each DR proceeded in the absence of DLT at the completion of Cycle 1 (treatment cycle=28 days for DR-A and 21 days for DR-B). Escalation to the next dose level within each DR was decided by a Safety Review Committee (SRC), consisting of the Principal Investigators, Sponsor's Medical Monitor, and Safety Physician representative, which reviewed all available safety information from all patients.

Within each Dose Regimen cohort, if no DLT was observed in a cohort, the subsequent patient group was enrolled at the next planned dose level of that dose regimen. If a DLT was observed in ≧2 of 3 patients at any dose level no further dose escalation occurred in that DR, and the current dose was defined as the maximum administered dose (MAD). If a DLT was observed in 1 of 3 patients in a cohort at any dose level, then up to 3 additional patients were enrolled in the same DR at that dose level. If a DLT was observed in 2 or more patients in the expanded cohort, then no further dose escalation occurred, and the current dose was defined as the MAD. After the MAD was defined, either the previously administered lower dose was expanded to a total of 6 patients, or an intermediate dose (between the MAD and the previous dose level) was investigated in a total of 6 patients. The highest dose tolerated in at least 5 of 6 patients was defined as the MTD or OBD.

The selection of dose regimen and dose level for up to 2 EXP cohorts was based on the MTD determination in Cycle 1, as well as the cumulative safety, efficacy and pharmacokinetic/pharmacodynamic profile of Aileron peptide-1 in subsequent treatment cycles in DEP.

Dose levels were not increased between cycles within each cohort, and patients were assigned only one dose level (i.e., no intra-patient dose escalation).

Statistical Methods

Results from DR-A and DR-B will be compared for all dose levels and patient groups.

Screening Assessments and Other Requirements Prior to Day 1 of Cycle 1

Molecular Screening Prior to Day 1 of Cycle 1: Molecular screening encompassed the following prior to the first administration of Aileron peptide-1 (Day 1 of Cycle 1): (i) collection of signed informed consent for molecular screening; (ii) collection of an archived tumor sample or a fresh tumor biopsy (unless a biopsy poses significant clinical risk) for p53 testing; (i) if confirmed to be p53 WT, the remainder of the tissue sample from enrolled patients was used to test for pharmacodynamic biomarkers. Confirmation of p53 WT status before administration of the first dose of Aileron peptide-1 was mandatory for enrollment in stage 1 of DEP for patients starting at Dose Level 4 and higher and stage 2 (if necessary) of DEP and EXP for all patients.

Molecular Screening Prior At Dose Level 4 and higher in Stage 1 of the DEP (as well as for all patients enrolled in Stage 2 of the DEP), molecular screening in patients with unknown p53 status was done prior to initiating the clinical screening. If the p53 status was known to be WT, these patients proceeded to clinical screening and were enrolled and receive Aileron peptide-1 before confirmation of p53 WT by the central laboratory.

In the EXP, patients had completed molecular screening at the central laboratory prior to proceeding to enrolment. These patients were only enrolled and received Aileron peptide-1 after confirmation of p53 WT by the central laboratory.

Clinical Screening within 21 Calendar Days Prior to Day 1 of Cycle 1 for DR-A and DR-B, all Dose Levels

The screening assessments and procedures performed within 21 calendar days (or as noted) prior to the first administration of Aileron peptide-1 (Day 1 of Cycle 1) included collection of signed informed consent, medical history (evaluation of baseline signs and symptoms), demographics, eligibility assessment, blood test for HIV, hepatitis B and C, vital signs (includes blood pressure, pulse, respiration rate, body temperature), physical examination, ECG, laboratory assessments including clinical chemistry (glucose, calcium, albumin, total protein, sodium, potassium, CO₂, chloride, phosphate, BUN [blood urea nitrogen], serum creatinine, uric acid, ALP, ALT, AST, total and direct bilirubin), hematology (complete blood count, platelets and differential), urinalysis (dipstick measurement [pH, specific gravity, protein, glucose, ketones, nitrite, leukocyte esterase] with microscopic analysis, if results of the dipstick indicate additional testing required), coagulation (PT, INR, aPTT), ECOG performance status, RECIST- (for solid tumor patients) or IWG- (for lymphoma patients) compliant imaging for disease assessment and tumor measurements as well as laboratory-based assays (e.g., prostate specific antigen) for patients with relevant disease indications, including a baseline PET-FDG and possibly FLT-PET scan(s), concomitant medications (current medications and those taken within 28 days of Cycle 1, Day 1).

Within 7 Calendar Days Prior to Day 1 of Cycle 1 for DR-A and DR-B, all Dose Levels

The screening assessments that was completed within 7 calendar days prior to the first administration of

Aileron peptide-1 (Day 1 of Cycle 1) included serum or urine pregnancy test (β-hCG) for women of child-bearing potential: performed within 2 days prior to first dose of Aileron peptide-1, confirm eligibility, vital signs, laboratory assessments—can be omitted if screening tests were performed within 7 days prior, ECOG performance status, and concomitant medications.

Requirements During Cycle 1 Day 1 of Cycle 1, for DR-A and DR-B, all Dose Levels

The study procedures that were performed prior to administration of Aileron peptide-1 included vital signs: within 30 minutes prior to SOI, physical exam, ECG: within 30 minutes prior to SOI (performed in triplicate (5-10 min between readings)), collection of blood for immunogenicity within 1 hr prior to SOI, collection of blood for all biomarker assessments within 1 hr prior to SOI, collection of blood for pharmacokinetic assessments: within 1 hr prior to SOI, and concomitant medications.

The study procedures that were performed after administration of Aileron peptide-1 included vital signs: (During infusion) 30 min (±3 min); (Post-infusion) At EOI (+5 min), and 1 (±5 min) and 2 hrs (±10 min) following EOI; ECG: At EOI (+5 min) and 1 hr (±5 min) and 2 hrs (±10 min) following EOI. Perform in triplicate (5-10 min between readings) only if patient has a QTc that is a) >500 msec; b) increased by 60 msec over pre-dose; or c) decreased by 50 msec below pre-dose recording; collection of blood for pharmacokinetic assessments: At EOI (+5 min), 30 min (±5 min) and 1 hr (±5 min), 2 (±10 min), 4 (±10 min) and 8 hrs (±10 min) following EOI; collection of blood for all biomarker assessments, EOI (+5 min) and 1 hr (±5 min) and 2, 4, and 8 hrs (±10 min) following EOI; concomitant medications; and adverse event (AE) assessment

Day 2 of Cycle 1, for DR-A and DR-B, all Dose Levels

The study procedures that were performed included vital signs, laboratory assessments, collection of blood for all biomarker assessments at 24 hr (±4 hr) after Day 1 SOI, collection of blood for pharmacokinetic assessments at 24 hr (±4 hr) after Day 1 SOI, concomitant medications, AE assessment, and TLS monitoring (via routine laboratory assessment sample)

Day 3 of Cycle 1, for DR-A and DR-B, all Dose Levels

The study procedures performed included vital signs, laboratory assessments (collection of blood for all biomarker assessments at 48 hr (±4 hr) after Day 1 SOI), collection of blood for pharmacokinetic assessments at 48 hr (±4 hr) after Day 1 SOI, concomitant medications and AE assessment.

Day 4 of Cycle 1, for DR-B ONLY, all Dose Levels

The study procedures performed prior to administration of Aileron peptide-1 included vital signs: within 30 minutes prior to SOI, physical exam, ECG: within 30 minutes prior to SOL Perform in triplicate (5-10 min between readings), laboratory assessments, collection of blood for immunogenicity within 1 hr prior to SOI, collection of blood for all biomarker assessments within 1 hr prior to SOI, collection of blood for pharmacokinetic assessments: within 1 hr prior to SOI, concomitant medications, and dverse Event (AE) Assessments

The study procedures performed after administration of Aileron peptide-1 included vital signs: (During infusion) 30 min (±3 min); (Post-infusion) At EOI (+5 min), and 1 and 2 hrs (±10 min) following EOI; ECG: At EOI (+5 min) and 1 hr (±5 min) and 2 hr (±10 min) following EOI. Perform in triplicate (5-10 min between readings) only if patient has a QTc that is a) >500 msec; b) increased by 60 msec over pre-dose; or c) decreased by 50 msec below pre-dose recording; laboratory assessments; collection of blood for all biomarker assessments within 1 hr after EOI; ollection of blood for pharmacokinetic assessments at EOI (+5 min), 30 min (±5 min) and 1 hr (±5 min), 2 (±10 min), 4 (±10 min) after EOI; concomitant medications and adverse event (AE) assessment

Day 8 of Cycle 1 for DR-A and DR-B, all Dose Levels

The study procedures performed prior to administration of Aileron peptide-1 included vital signs: within 30 minutes prior to SOI; physical exam; laboratory assessments, collection of blood for all biomarker assessments within 1 hr prior to SOI, collection of blood for pharmacokinetic assessments within 1 hr prior to SOI, ECOG performance status, concomitant medications and AE assessment.

The study procedures performed after administration of Aileron peptide-1 include vital signs: (During infusion) 30 min (±3 min); (Post-infusion) At EOI (+5 min), and 1 hr (±5 min) and 2 hrs (±10 min) following EOI; collection of blood for all biomarker assessments within 1 hr after EOI; collection of blood for pharmacokinetic assessments at EOI (+5 min) and 30 min (±5 min), 1 hr (±5 min), 2 and 4 hrs (±10 min) after EOI; concomitant medications and AE assessment.

Day 15 for DR-A and Day 11 for DR-B of Cycle 1

The study procedures performed prior to administration of Aileron peptide-1 included vital signs: within 30 minutes prior to SOI; physical exam; laboratory assessments; collection of blood for all biomarker assessments within 1 hr prior to SOI; collection of blood for pharmacokinetic assessments within 1 hr prior to SOI; ECOG performance status; concomitant medication and AE assessment.

The study procedures performed after administration of Aileron peptide-1 included vital signs: (During infusion) 30 min (±3 min); (Post-infusion) At EOI (+5 min), and 1 hr (±5 min) and 2 hrs (±10 min) following EOI; collection of blood for pharmacokinetic assessments At EOI (+5 min) and 30 min (±5 min), 1 hr (±5 min); 2, 4, and 8 hrs (±10 min) after EOI; collection of blood for all biomarker assessments within 1 hr at EOI (+5 min); EOI plus 1 hr (±5 min); 4, and 8 hr (±10 min) after EOI; concomitant medications; and AE assessment.

Day 16 DR-A and Day 12 DR-B for Cycle 1

The study procedures performed included vital signs; laboratory assessments; collection of blood for biomarker assessments: at 24 hr (±4 hr) after SOI on the day prior; only for patients with a successful study biopsy performed prior to start of study medication: Needle biopsy for biomarker assessments- to be performed within 48 hours of Cycle 1, Day 15 (DR-A) or Day 11 (DR-B) infusion OR Cycle 2, Day 15 (DR-A) or Day 11 (DR-B) infusion, at the discretion of the Investigator (unless the biopsy poses significant risk to the patient); collection of blood for pharmacokinetic assessments at 24 hr (±4 hr) after Day 15 (DR-A) or Day 11 (DR-B) SOI; collection of blood for all pharmacodynamic assessments at 24 hr (±4 hr) after SOI on the day prior; concomitant medications; cAE assessment; and FLT-PET for patients who received FLT-PET at screen and have SUV≧5.

Day 22 for DR-A and Day 18 for DR-B or of Cycle 1

The study procedures performed included vital signs; laboratory assessments—hematology only; collection of blood for all biomarker assessments; concomitant medications; and AE assessment.

Day 29 for DR-A and Day 22 for DR-B of Cycle 1 (−1 Day Up to +3 Days)/Cycle 2 Day 1

Procedures listed below under Requirements During Subsequent Cycles Beginning with Cycle 2 were performed. Note: “Day 22 or 29”=Day 1 of next cycle for patients continuing treatment. Cycle 1 Day 22 or 29/Cycle 2 Day 1 pre-dose evaluations were to be done within 3 days prior to next cycle drug administration.

If the patient was not continuing treatment beyond Cycle 1 the procedures listed below under End-of-Study Visit section were performed.

Requirements During Subsequent Cycles Beginning with Cycle 2

Day 29 for DR-A and Day 22 for DR-B of prior cycle/Day 1 of Cycle 2 and subsequent cycles Note: “Day 22 or 29”=Day 1 of next cycle for patients continuing treatment. Day 22 or 29 of prior cycle/Day 1 of current cycle pre-dose evaluations were done within 3 days prior to drug administration.

Note: Blood samples to evaluate CTC were not collected in Cycle 2 or subsequent cycles.

The study procedures performed prior to administration of Aileron peptide-1 included vital signs: within 30 minutes prior to SOI; physical exam; ECG: within 30 minutes prior to SOL Perform in triplicate (5-10 min between readings); laboratory assessments; collection of blood for immunogenicity: within 1 hr prior to SOI; collection of blood for biomarker assessments (MIC-1 only): within 1 hr prior to SOI; collection of blood for pharmacokinetic assessments (Cycle 2 Only): within 1 hr prior to SOI; ECOG performance status; concomitant medications; and AE assessment.

The study procedures performed after administration of Aileron peptide-1 included vital signs: (During infusion) 30 min (±3 min); (Post-infusion) at EOI (+5 min) and as clinically indicated following EOI; ECG: at EOI (+5 min) Perform in triplicate (5-10 min between readings) only if patient has a QTc that is a) >500 msec; b) increased by 60 msec over pre-dose; or c) decreased by 50 msec below pre-dose recording; collection of blood for biomarker assessments (MIC-1 only): within 1 hr after EOI; collection of blood for pharmacokinetic assessments (Cycle 2 Only): At EOI (+5 min) and 30 min ((±5 min), 1 hr (±5 min), 2 and 4 hrs (±10 min) after EOI; concomitant medications; and AE assessment.

Day 8 of DR-A and Days 4 and 8 of DR-B of Cycle 2 and Beyond

The study procedures performed prior to administration of Aileron peptide-1 included vital signs: within 30 minutes prior to SOI; physical exam; laboratory assessments-hematology only; ECOG performance status; concomitant medications; and AE assessment.

The study procedures performed after administration of Aileron peptide-1 included vital signs: (During infusion) 30 min (±3 min); (Post-infusion) at EOI (+5 min) and as clinically indicated following EOI; concomitant medications; and AE assessment.

Day 15 of DR-A and Day 11 of DR-B of Cycle 2 and Beyond

The study procedures performed prior to administration of Aileron peptide-1 included vital signs: within 30 min prior to SOI; physical exam; laboratory assessments; collection of blood for biomarker assessments (MIC-1 only): within 1 hr prior to SOI; collection of blood for pharmacokinetic assessments (Cycle 2 Only): within 1 hr prior to SOI; ECOG performance status; concomitant medications; and AE assessment.

The study procedures performed after administration of Aileron peptide-1 included: vital signs: (During infusion) 30 min (±3 min); (Post-infusion) at EOI (+5 min) and as clinically indicated following EOI; collection of blood for biomarker assessments (MIC-1 only): within 1 hr after EOI; collection of blood for pharmacokinetic assessments (Cycle 2 Only) at EOI (+5 min) and 30 min (±5 min), 1 hr (±5 min), 2 and 4 hrs (±10 min) after EOI; concomitant medications and AE assessment.

Day 16 DR-A and Day 12 of DR-B of Cycle 2 and Beyond

The study procedures performed included vital signs, laboratory assessments, collection of blood for biomarker assessments: at 24 hr (±4 hr) after Day 15 or 11 SOL collection of blood for pharmacokinetic assessments (Cycle 2 Only): at 24 hr (±4 hr) after Day 15 or 11 SOL concomitant medications, and AE assessment.

After Even Numbered Cycles

Blood was collected for immunogenicity. Tumor assessment was performed following same procedure used for baseline measurement, for example imaging, physical exam as well as laboratory-based assays (e.g., prostate specific antigen) for patients with relevant disease indications.

For patients who achieved “Stable Disease” as defined by RECIST or IWG criteria, a FDG-PET scan was indicated, provided that an evaluable FDG-PET-scan was performed prior to starting treatment with study drug.

CT Imaging

All patients receive a CT image prior to the first dose. After dosing commences in Dosing Regimen-A (DR-A), CT images will be obtained at the end of Cycle 2 and every other cycle thereafter in DR-A, e.g., Cycles 4, 6, and 8. In Dosing Regimen-B (DR-B) CT images will be obtained after the last infusion in Cycle 3 and every third cycle thereafter in DR-B, e.g., Cycles 6, 9, and 12. Images will be obtained after the last dose is administered in those cycles but prior to the Day 18 visit.

End-of-Study Visit

The end-of-study visit was to be conducted 30 (±2) calendar days after the last administration of Aileron peptide-1 or withdrawal from the study. The study procedures performed included serum or urine pregnancy, vital signs, physical exam, ECG, laboratory assessments, collection of blood for immunogenicity, collection of blood for biomarker assessment, collection of blood for pharmacokinetic assessment, ECOG performance status, tumor assessment following same procedure used for baseline measurement, for example imaging, physical exam as well as laboratory-based assays (e.g., prostate specific antigen) for patients with relevant disease indications, concomitant medication and AE assessment.

Pharmacodynamic Assessment

Blood samples for pharmacodynamic assessments were collected at the following timepoints:

TABLE 12 Cycle 1 and Cycle 2 Dose Regimen Pharmacodynamic Assessments Dose Regimens Assessment Blood Sample Collection Schedule Cycle 1 DR-A, DR-B, or Both: Day 1-Both (pre) MIC-1 and within 1 hour before the start of CTC infusion (SOI) Day 1-Both (post) Samples EOI (+ 5 min) & EOI + 1 hr (±5 min), 2, 4, and 8 hr (±10 min) Day 2-Both 24 hours (±4 hr) after SOI on Day 1 Day 3-Both 48 hours (±4 hr) after SOI on Day 1 Day 8 DR-A within 1 hour before SOI and Day 4 & 8 DR-B within 1 hour after the end of infusion (EOI) Day 15 DR-A within 1 hour before SOI and Day 11 DR-B within 1 hour after EOI Day 15 DR-A within 1 hour before SOI and Day 11 DR-B EOI (+ 5 min) & EOI + 1 hr (±5 min), 2, 4, and 8 hr (±10 min) Day 16 DR-A 24 hours (±4 hrs) after SOI day prior Day 12 DR-B Day 22 DR-A During Day visit Day 18 DR-B Each Subsequent Cycle Starting in Cycle (Cy) 2 Cy 1 Day 29 MIC-1 Only within 1 hour before SOI and DR-A Cy 1 Day 23 within 1 hour after EOI DR-B = Cycle 2 Day 1 Day 15 DR-A within 1 hour before SOI and Day 11 DR-B within 1 hour after EOI Day 16 DR-A 24 hours (±4 hrs) after SOI day prior Day 12 DR-B End of study visit During end of study visit NOTE: no pharmacodynamic assessments for solid tumors or lymphoma on Day 8 DR-A or Days 4 and 8 DR-B

Pharmacokinetic (PK) Assessments

Blood samples for pharmacokinetic assessment were collected at the following timepoints:

TABLE 13 Cycle 1 and Cycle 2 Dose Regimen Pharmacokinetic Assessments Cycle 1 Day 1 within one hour before SOI DR-A and DR-B EOI (+5 min) 30 min after EOI (±5 min) 1 hr after EOI (±5 min) 2 hr after EOI (±10 min) 4 hr after EOI (±10 min) 8 hr after EOI (±10 min) Day 2 24 hours (±4 hr) after SOI day prior DR-A and DR-B Day 3 48 hours (±4 hr) after SOI Day 1 DR-A and DR-B Day 8, DR-A within one hour before SOI Days 4 & 8, DR-B EOI (+5 min) 30 min after EOI (±5 min) 1 hr after EOI (±5 min) 2 hr after EOI (±10 min) 4 hr after EOI (±10 min) Day 15, DR-A within one hour before SOI Day 11, DR-B EOI (+5 min) 30 min after EOI (±5 min) 1 hr after EOI (±5 min) 2 hr after EOI (±10 min) 4 hr after EOI (±10 min) 8 hr after EOI (±10 min) Day 16, DR-A 24 hours (±4 hrs) after SOI day prior Day 12, DR-B Cycle 2 Cycle 1 Day 29/ within one hour before SOI Cycle 2 Day 1, DR-A EOI (+5 min) Cycle 1 Day 23/ 30 min after EOI (±5 min) Cycle 2 Day 1, DR-B 1 hr after EOI (±5 min) 2 hr after EOI (±10 min) 4 hr after EOI (±10 min) Day 15, DR-A within one hour SOI Day 11, DR-B EOI (+5 min) 30 min after EOI (±5 min) 1 hr after EOI (±5 min) 2 hr after EOI (±10 min) 4 hr after EOI (±10 min) Day 16, DR-A 24 hours (±4 hrs) after SOI day {close oversize brace} Cycle 2 Only prior Day 12, DR-B End of study visit During end of study visit NOTE: no PK assessments on Day 8 in DR-A or Days 4 and 8 in DR-B

Example 4 Further Studies

Aileron peptide-1 was evaluated for safety, tolerability, pharmacokinetics and pharmacodynamics in adult patients with advanced solid tumors or lymphomas expressing WT p53 that are refractory to or intolerant of standard therapy, or for which no standard therapy exists. FIG. 6 shows one way Aileron peptide-1 was designed to inhibit MDMX and/or MDM2, which leads to reactivation of WT p53.

Aileron peptide-1 was able to penetrate the cell membrane and localize within the nucleus. Further Aileron peptide-1 can disrupt protein-protein interactions within the cell such as the interactions between p53 and MDM2 and MDMX.

Several in-vivo and in-vitro studies of Aileron peptide-1 were conducted. In these studies, Aileron peptide-1 binded to both MDM2 and MDMX with nanomolar affinities and demonstrated evidence of specific on-target mechanism in vitro by gene expression profiling. In addition, Aileron peptide-1 demonstrated tumor growth suppression, p53-dependent cell cycle arrest, apoptosis and anti-tumor activity in an MDM2/MDMX-overexpressing xenograft cancer model with clear correlation to on-target pharmacokinetic and pharmacodynamic, or pharmacokinetic/pharmacodynamic, activity.

Dose escalation phase were designed to evaluate Aileron peptide-1 in patients with solid tumors or lymphoma. The dose escalation phase was not limited by type of tumor or lymphoma. Aileron peptide-1 was administered to patients with sarcoma, gastric cancer, non-small cell lung cancer, ovarian cancer and thymoma. In some cases Aileron peptide-1 was used to treat tumors and lymphomas in which WT p53 is prevalent in greater than 50% of patients. p53 wild-type status is prevalent in greater than 50% of patients suffering from at least 19 different tumor types. Thus, indication potential can vary from orphan indications or large market opportunities. See e.g., FIG. 7.

p53 signal activation study was conducted to determine if Aileron peptide-1 had a differential effect on cancer cell lines with mutant p53 compared to WT p53. In the study, we measured the effect of Aileron peptide-1 in 312 cell lines across a variety of different cancers to compare the effect of Aileron peptide-1 in cell lines with mutant p53 and cell lines with WT p53. See FIG. 8. In the 207 mutant p53 cell lines, Aileron peptide-1 had no discernable effect, but in the 105 WT p53 cell lines, nearly all showed tumor cell death. See FIG. 8. The WT p53 cell lines that did not show tumor cell death included WT p53 cell lines associated with Human Papilloma Virus, or HPV, related cancers, such as cervical and head and neck. By concentrating on WT p53 and responsive tumors, we are able to predict patient populations that can have a better chance of response from our product candidate.

In another study, the binding affinity of Aileron peptide-1 for MDM2 or MDMX relative to the binding affinity for MDM2 and MDMX of WT p53 and of an MDM2 small molecule inhibitor was measured. The affinity of a drug to a receptor is the measure of how effectively that drug binds to its target and can provide insight on the potential for on-target effect and off-target toxicity. Aileron peptide-1 was designed to bind to MDM2 and/or MDMX with a higher affinity than WT p53 so that Aileron peptide-1 disrupts the binding of MDM2 and/or MDMX to WT p53 by binding to MDM2 and/or MDMX in lieu of p53. Such binding can enable p53 to be released and activated. In this study, we also measured a small molecule MDM2 inhibitor's binding affinity to MDMX, which showed no binding to this target. Table 14 below shows Aileron peptide-1's ability to bind to MDM2 and MDMX relative to WT p53 and the small molecule MDM2 inhibitor.

TABLE 14 Aileron peptide-1's ability to bind to MDM2 and MDMX relative to WT p53 and the small molecule MDM2 inhibitor. Kd, nM WT p53 Aileron peptide-1 MDM2 Inhibitor MDM2 770 13.7 9.8 MDMX 480 8.9 >3000

In Vivo

We studied the effects of Aileron peptide-1 in both solid tumors. In the study depicted FIGS. 9a and 9b , we evaluated the effect of Aileron peptide-1 administered by an intravenous, or IV, injection in an MDMX-driven MCF-7 breast cancer xenograft model. In this study, we evaluated different doses, schedules and durations of treatment with Aileron peptide-1 and vehicle to determine effect on tumor volume growth. Aileron peptide-1 showed statistically significant tumor growth inhibition at doses ranging from 2.5 mg/kg to 5 mg/kg to 10 mg/kg and 20 mg/kg when these doses were administered twice a week for a 28 day period. See FIGS. 11a and 11 b.

Toxicology and Nonclinical Safety Experiments

The pivotal 4-week multiple-dose GLP studies in rats and monkeys utilized twice-weekly IV dosing rather than the once-weekly IV dosing planned as the initial clinical regimen. The studies provided dose- and exposure-related assessments during both dosing and recovery periods, and results were utilized to define the maximum tolerated doses (MTD) and estimate the severely toxic dose for 10% (STD₁₀) of rats and the highest non-severely toxic dose (HNSTD) in monkeys. All gross and microscopic signs of intolerance (e.g., reduced organ weights, sporadic findings of multi-tissue hemorrhage and hepatic necrosis) and changes in serum chemistry parameters were considered as secondary to red blood cell (RBC), platelet and/or white blood cell (WBC) depletions or anorexia and dehydration in both species. Recovery assessments revealed regenerative and compensatory changes consistent with marrow cell survival and reversibility of all related hematologic and secondary toxicities.

The DLT in both animal species appears to be related to the suppression of hematopoietic cells in the bone marrow, in particular cells of the megakaryocyte lineage, resulting in significant decreases in peripheral blood platelets that demonstrated recovery upon the cessation of dosing. See FIG. 7.

The STD₁₀ in rats was defined at 10 mg/kg based on the mortality of one animal in a satellite group for hematology sampling during recovery. The HNSTD in monkeys was defined at 5 mg/kg, based on a complete lack of significant thrombocytopenia at this lowest dose level. However, almost all of the monkeys at the mid- and high-dose levels tolerated Aileron peptide-1 administration well; only one animal at each of these dose levels developed significant thrombocytopenia (<100,000×10⁶/ml).

Rats are more sensitive to the bone marrow and hematologic effects of Aileron peptide-1 than monkeys on the basis of exposures at maximally tolerated doses. Exposure at rat STD₁₀ (AUC_(0-∞)=562 μg·hr/mL at 10 mg/kg) was below that of HNSTD in monkeys (AUC_(0-∞)=813 μg·hr/mL at 5 mg/kg). These in vivo results correlate with those obtained from in vitro hemotoxicity assays via luminescence output (HALO). In these investigations, Aileron peptide-1 in general inhibited the induced proliferation of bone marrow precursor cells from rats to a greater extent than those from monkeys or humans. IC₅₀ values were ˜2- to 8-fold higher for rat cells than for monkey or human cells, with the largest difference noted for megakaryocyte colony forming cells, the platelet precursors. These results correlate with in vivo findings indicating that rats are more sensitive to the bone marrow and hematologic effects of Aileron peptide-1 than monkeys on the basis of dose and exposures at maximally tolerated doses. These results also suggest that, in terms of projecting potential bone marrow and hematological toxicity levels in humans, the monkey pharmacokinetic-pharmacodynamic data can be more clinically relevant than the rat data.

Aileron peptide-1 was negative in genetic toxicology studies, including bacterial mutagenicity (Ames), chromosomal aberrations (human peripheral blood lymphocyte) and in vivo micronucleus (rat bone marrow) assays. Safety pharmacology studies were performed to assess the effects of Aileron peptide-1 on hERG potassium channels in vitro and on cardiac function in cynomolgus monkeys. There were no significant adverse findings in these studies.

Compared to the twice-weekly IV dosing schedule utilized in the 4-week GLP toxicity studies, the first-in-human clinical trial of Aileron peptide-1 will initially assess once-weekly IV dosing for three weeks. In addition, the demonstrated reversibility of Aileron test peptide-1-induced hematologic effects, the ability to detect such findings with routine laboratory measurements, and the availability of effective supportive therapies, all provide additional safety margin in the clinic.

Pharmacokinetics and Absorption, Distribution, Metabolism and Excretion

In rats, Aileron peptide-1 generally showed linear, dose-proportional increases in C_(max) and AUC. In the 4-week rat GLP toxicity study, C_(max) of Aileron peptide-1 ranged from 49.9 to 186 μg/mL, AUC_(0-∞) ranged from 90.5 to 562 μg·hr/mL, and clearance ranged from 19.2 to 28.3 mL/hr/kg. Half-life (t_(1/2)) values could not be calculated due to variable coefficients of determination (r²<0.9).

In non-human primates, Aileron peptide-1 generally showed exposures that increased proportionally with dose, although an apparent plateau in exposure was observed at the high-dose group (20 mg/kg) in the 4-week monkey GLP toxicity study. In the study, C_(max) of Aileron peptide-1 ranged from 133 to 562 μg/mL, t_(1/2) ranged from 3.7 to 6.0 hrs, AUC_(0-∞) ranged from 813 to 1,600 μg·hr/mL, and clearance ranged from 6.5 to 13.8 mL/hr/kg.

No significant sex-based differences in pharmacokinetic parameters were observed in either rats or monkeys, and no accumulation was observed following repeated doses on a twice-weekly schedule in the GLP toxicity studies.

Proteolysis is the expected major biotransformation pathway of Aileron peptide-1. The predominant metabolite, Aileron peptide metabolite-1, is a 3-amino acid truncation with the cyclic peptide portion intact, and the same metabolite profile was noted in in vitro stability studies with monkey, rat, mouse and human cryopreserved hepatocytes. In a single-dose rat study, hepatobiliary metabolism and elimination represented the predominant clearance pathway for Aileron peptide-1, with Aileron peptide metabolite-1 as the major excretion product observed in the bile.

In vitro studies revealed that Aileron peptide-1 is not an inhibitor of any cytochrome P450 (CYP) isoforms tested. In vitro assays for CYP induction also did not indicate any significant treatment-related effects with Aileron peptide-1. Based on these findings, the potential of clinically relevant drug-drug interactions for concomitant medications that are cleared through CYP-mediated mechanisms is deemed to be low.

Aileron peptide-1 was tested in vitro against common transporters, and >90% inhibition of organic anion transporter polypeptide (OATP) members OATP1B1 and OATP1B3 and bile salt export pump (BSEP) at concentrations that can be clinically relevant (e.g., at C_(max) of high-dose levels) was observed. Based on these findings, the potential of clinically relevant drug-drug interactions by Aileron peptide-1 with medications (e.g., methotrexate, statins) that are significantly cleared by hepatobiliary transporters should be considered.

In Vivo

An open-label, multi-center, dose-escalation, two-arm study was used to design to evaluate the safety, tolerability, pharmacokinetic, pharmacodynamic and anti-tumor effects of Aileron peptide-1 administered by intravenous (IV) infusion in patients with advanced solid tumors or lymphomas expressing WT p53 that are refractory to or intolerant of standard therapy, or for which no standard therapy exists. The study included a dose escalation phase to establish the maximum tolerated dose, or MTD, or the optimum biologic dose, or OBD, of Aileron peptide-1, and a dose expansion phase to investigate the clinical safety profile and potential efficacy of Aileron peptide-1 at the MTD or OBD. In the expansion phase of the study, Aileron peptide-1 was studied in distinct groups of patients with specific solid tumors or lymphomas. The selection of the solid tumors or lymphomas was finalized based on results of the dose escalation phase, as well as data from additional nonclinical pharmacology studies. The latter included the investigation of multiple solid cancer cell lines such as breast, bladder, head/neck, gastrointestinal, or GI, liver, lung, pancreas, prostate and sarcoma to facilitate the comparison of cell line sensitivity to Aileron peptide-1 across and within tumor types. Treatment of patients in the dose escalation and the dose expansion phases of the trial continued until documentation of disease progression, unacceptable toxicity, or patient or physician decision to discontinue therapy.

The dose escalation phase is based on a “3+3” dose escalation design. In the dose escalation phase, patients in the first two dose levels received Aileron peptide-1 once a week for three weeks every 28 days. Patients in the higher dose levels received Aileron peptide-1 either once weekly for three consecutive weeks for a 28-day cycle or twice weekly for two consecutive weeks for a 21-day cycle. See FIG. 10.

Patients with solid tumors or lymphoma were enrolled in the dose escalation phase who had exhausted standard therapies or for whom standard therapies are not available, completed enrollment up to dose group 4b and are enrolled patients in dose group 5a. Patients suffering from cancers with known HPV-association were excluded from enrollment, because HPV is known to deactivate WT p53. The tumor types included as of such date are non-small cell lung cancer, various types of sarcoma, cholangiocarcinoma, cystic adenoid carcinoma, follicular non-hodgkin lymphoma, thymoma, prostate cancer, endometrial cancer, and ovarian cancer. Since our trial was primarily safety and tolerability focused, we started dosing at relatively low dose levels and the protocol did not require patients in the first three dose levels to be p53-wildtype or HPV-negative.

To identify specific p53 patients for our trial, we employed a central laboratory to test both archived tumor tissue samples and fresh biopsy samples from patients enrolled in the trial for p53 status using Next-Generation Sequencing. 12 of 13 patients enrolled in those dose levels were confirmed to have WT status. Starting in dose level 4, WT p53 status was a mandatory eligibility criterion.

In this trial, clinical activity or response to Aileron peptide-1 was assessed through the use of both pharmacodynamic biomarkers and imaging assessment. Pharmacodynamic biomarkers provided us with information as to on-target activity, specific patient type response and early insight as to effect on tumor. As part of the trial, we were also assessing the effect of Aileron peptide-1 on potential Pharmacodynamic biomarkers in various different sources of biological samples such as tumor biopsies, circulating tumor cells where detectable, mononuclear blood cells and blood samples. Dependent on the sample type, those pharmacodynamic biomarkers include measurements of MDMX, MDM2, p21, p53, apoptosis and macrophage inhibitory cytokine-1, or MIC-1. In addition, we received standard imaging assessments, such as computed tomography, or CT, magnetic resonance imaging, bone scans and PET scans from patients, depending on number cycles administered. CT-imaging was performed at the end of cycle 2, and every two cycles thereafter in the 28-day cycle group and at the end of cycle 3 and every three cycles thereafter in the 21-day cycle group. We were measuring anti-tumor activity using RECIST for patients with solid tumors and 2014 International Working Group, or IWG, criteria for patients with lymphomas, enabling us to objectively evaluate whether a tumor has progressed, stabilized or shrunk. In addition, anti-tumor effects can be determined by physical examination or clinically validated serum tumor markers.

Pharmacokinetic Profile

Aileron peptide-1 was delivered systemically in an IV administration given potential advantages of avoiding metabolic impact from hepatic and gastrointestinal enzymes as well as ability for reproducible systemic bioavailability with dose escalation. As shown in the FIG. 11a , drug concentration was measured in dose levels for Cohorts 1 (0.16 mg/kg), 2 (0.32 mg/kg), 3a (0.64 mg/kg), 3b (0.32 mg/kg), 4a (1.25 mg/kg). In patients, Aileron peptide-1 has consistently produced a dose dependent increase in maximum drug serum concentration observed, or Cmax, as well as longer corresponding half-life of between eight and 10 hours. This half-life is adequate to re-activate WT p53 and begin the process of initiating the regulation of the transcription of genes.

Aileron peptide-1 shows reproducible profiles from patient to patient and dose-to dose enabling exposure projections for higher dose levels to predict efficacy and safety. FIG. 11b shows the measured drug concentration in dose levels 1 (0.16 mg/kg), 2 (0.32 mg/kg) and 3 (0.64 mg/kg); and projected for dose levels 4 (1.25 mg/kg), 5 (2.5 mg/kg), and 6 (5.0 mg/kg).

FIG. 12 shows the pharmacokinetic model of Aileron peptide-1. The peptide shows nonlinear Michaelis-Menten clearance and linear elimination.

Safety Results

Aileron peptide-1 was considered to be well tolerated at all dose levels by the investigators. There were no reported dose-limiting toxicities nor study-related serious adverse events. Looking at non-hematologic safety, the most common related adverse events are nausea and fatigue. Looking at hematologic safety, the first two dose levels 1 and 2 showed no cytopenias during cycles 1 and 2, whereas at dose levels 3A, 3B and 4A, patients showed drug-related events of mild to moderate anemia, mild thrombocytopenia and mild neutropenia. One patient at dose level 3B experienced a grade 4 neutropenia which Investigators reported as probably related to study medication. The patient's complete blood count presented trough values of grade 2 leukocytopenia, grade 1 anemia and grade 1 thrombocytopenia. Two concomitant medications were initiated around the same time that treatment with Aileron peptide-1 was started, both of which have been suspected to be associated with the occurrence of neutropenia. There was no association between the patient's neutropenia and drug exposure, the patient's last complete blood count showed an improvement to grade 3 neutropenia, no treatment was administered for neutropenia and no infectious complications were reported.]

4 formal Safety Review Meetings with Investigators confirm no DLTs. For DL1, 2 and 3A there was an unanimous decision to escalate at double the dose. For DL3B, there was an unanimous decision to escalate via Fibonacci in DL4B. New Dose may be 0.53 mg/Kg instead of 0.64 mg/Kg.

Hematologic and non-hematologic adverse events were generally consistent with our preclinical toxicology profile:

-   -   No genotoxicity     -   No immunogenicity     -   No relevant findings in cardiovascular safety     -   No relevant findings suggestive of GI toxicity     -   No Myelosuppression as the dose-limiting toxicity

Biomarker Assessments

In the dose escalation phase, we used several exploratory biomarkers to confirm Aileron peptide-1's pharmacological or on-target biological activity, aid patient recruitment and help inform dose selection.

Pharmacodynamic biomarkers were received on MDMX, MDM2, p21, p53, apoptosis and MIC-1. The first biomarker for which we received data is MIC-1. MIC-1 is a secreted p53-regulated cytokine that is readily measured in blood if p53 is activated, and can serve as a biomarker for p53 activation. Under normal conditions, p53 expression remains low, resulting in corresponding negligible levels of MIC-1. However, when WT p53 activation occurs in response to a tumor, this also leads to increased levels of MIC-1. We measured MIC-1 one hour before initial infusion and again 24 hours after initial infusion. In patients at dose levels ranging from dose level 1 to dose level 4A, we observed a statistically significant dose dependent response in the increase of MIC-1. See FIG. 13.

Further, mononuclear blood cells from 4 patients confirmed that Aileron peptide-1 penetrates cell membrane and activates p53-signalling. We measured the amount of intracellular p53 and p21 in mononuclear blood cells from 4 patients at: (a) end of infusion of Aileron peptide-1, (b) 1 hour after the end of infusion of Aileron peptide-1 and (c) 4 hour after the end of infusion of Aileron peptide-1. As seen in FIG. 14, a 1.8 times increase in the levels of intracellular p53 and about 3 times increase in the levels of intracellular p21 was observed.

Thus, we conclude that Aileron peptide-1 is penetrating the cell membrane, localizing within the nucleus and releasing WT p53. An increase of at least eight fold in MIC-1 levels from baseline serves as guidance for the minimum dose needed for p53 re-activation.

Overall, at least two independent biomarker studies support Aileron peptide-1-mediated activation of intracellular p53 signaling: (i) MIC-1 serum-protein (as measured by ELISA): dose-response relationship, and (ii) p53 and p21 increase (as measured by flow-cytometry) in blood cells.

Efficacy

Objective tumor response is an endpoint for efficacy in trials. Patients in the 28-day cycle group are measured at baseline and again after two cycles of therapy, or approximately within 56 days following initial dosing. Patients in the 21-day cycle group are measured at baseline and again after three cycles of therapy, or approximately within 63 days following initial dosing. RECIST criteria definitions are as follows:

-   -   Stable Disease, or SD: Neither sufficient shrinkage to qualify         for partial response nor sufficient increase to qualify for         progression, taking as reference the smallest sum diameters         while on study.     -   Partial Response, or PR: At least a 30% decrease in the sum of         the diameters of target lesions, taking as reference the         baseline sum diameters.     -   Complete Response, or CR: Disappearance of all target lesions.         Any pathological lymph nodes, whether target or non-target, must         have reduction in short axis to less than 10 millimeters.

Tests show that patients who have completed at least two cycles of treatment, some patients have stable disease. Aileron peptide-1 has shown a stable disease rate. See FIG. 15.

Table 15 below shows exemplary patients who were treated with Aileron peptide-1. These patients encompassed a range of solid tumors with either wild type or mutant p53. As seen in Table 16, after 2/3 cycle treatment each of the patient 4, 5, 7, 8, 10, 11 and 15 have stable disease, while only patients 2, 6 and 12 showed a progressive disease. After completing 3/4 treatment cycles, patient 11 continued to show stable disease. As used here, stable disease refers to the situation where there is neither a sufficient shrinkage of the tumor to qualify for partial response nor sufficient increase to qualify for progression, taking as reference the smallest sum diameters while on study.

TABLE 15 Patient information Tumor Tumor Patient P53 NGS Tissue(s) Size Burden No. 1° Cancer Histopath 2° Cancer WT Tested Organ mm mm 1 Salivary gland squamous cell UNK liver Lymph node 30 55 Right Hepatic 25 Lobe Posterior 2 liposarcoma liposarcoma Yes retroperitoneal: soft tissue 48 48 mass 3 Gall bladder adenocarcinoma Yes Gall bladder liner 16 36 endoperitoneal 20 4 Submandibular Adenoid cystic Yes adenoid oropharynx 43 65 adenocarcinoma Carcinoma lung 22 5 liposarcoma Liposarcoma Yes liposarcoma retroperitoneal 175 301 retroperitoneal 126 6 GIST (sarcoma) GASTROINTESTINAL UNK N/A MESENTRIC 25 135 STROMAL TUMOR MASS lung 20 lung 16 liver 84 7 NSCLC invasive Brain/head UNK N/A lung 10 71 andenocarcinoma Lymph node 20 lung 20 Lymph node 21 8 liposarcoma Basal Cell Yes tumor resection- Stomach 147 443 retroperitoneal Stomach 127 lymph node Bone 155 Liver 14 9 prostate Adenocarcinoma UNK N/A Lymph node 48 86 liver 15 Lymph node 23 10 NSCLS Stage IV Yes right lung Lymph node 15 99 adenocarcinoma the left nodule Lymph node 21 lung Lymph node 21 Lung 25 Lung 17 11 ovarian met. ov cancer stage iv No Tumor Liver 17 64 ca with liver mets resection- Liver 30 uterus Other 17 12 endometrial ENDOMETRIAL No Liver 13 78 SEROUS Liver 17 CARCINOMA Lymph node 18 Lymph node 20 13 breast Carcinoma osteosarcoma Yes Tumor lung 64 181 resection- lung 117 osteosarcoma 14 leiomyosarcoma Unknown UNK Lung 54 195 Liver 12 Liver 99 Liver 30 15 leiomyosarcoma Uterine Yes Lymph node 44 76 Lymph node 32 16 lymphona b-cell lymphoma- Lymph node 300 follicular (CT & PET) 17 thymoma

TABLE 16 Patient response after treatment with Aileron Peptide -1 for 2/3 cycle Tumor Tumor % change Patient Size Burder from New No. Organ mm mm bsln Lesions? Target Non-Target Overall 1 Lymph node Off Study: Right Hepatic Non- Lobe Posterior compliance 2 soft tissue mass 62 62   29% No Progression Not Done Progressive Disease 3 liner Off Study: endoperitoneal CDP 4 oropharynx 45 69    6% Yes Stable Progressive Stable lung 24 Disease Disease Disease 5 retroperitoneal 186 336  11.2% NO Stable Not done Stable retroperitoneal 150 Disease Disease 6 MESENTRIC 29 159  17.8% Yes Stable Non-complete Progressive MASS (SUPERIOR Disease Response/Non- Disease lung 11 HEPATIC progression lung 19 LOBE UP liver 100 TO 1.5 CM) 7 lung 13 77    8% No Stable Non-complete Stable Lymph node 20 Disease Response/Non- Disease lung 20 progression Lymph node 24 8 Stomach 157 518  16.9% No Stable Progressive Stable Stomach 145 Disease Disease Disease Bone 180 Liver 36 9 Lymph node 53 122 41.86% No Progressive Non-Complete Off Study: liver 35 Disease Response/Non- Objective Lymph node 34 Progression Disease Progression 10 Lymph node 21 116 17.20% No Stable Not done Stable Lymph node 24 Disease Disease Lymph node 24 Lung 28 Lung 19 11 Liver 17 71 10.90% No Stable Not done Stable Liver 24 Disease Disease Other 30 12 Liver 15 100 28.21% Yes Progression Not all Progressive Liver 19 (LIVER Evaluated or Disease Lymph node 32 LESION) Not Assessable Lymph node 32 13 lung — — — lung — 14 Lung 69 233 19.48% Yes (left Not Not Not Liver 19 subhepatic entered entered entered Liver 105 mass) yet yet yet Liver 40 15 Lymph node 44 77  1.30% No Stable Non-complete Stable Lymph node 33 Disease Response/Non- Disease progression 

1.-227. (canceled)
 228. A method of treating a solid tumor that lacks a p53 deactivating mutation, in a human subject in need thereof wherein the method comprises administering to the human subject a pharmaceutical composition comprising a therapeutically effective amount of a peptidomimetic macrocycle or a therapeutically equivalent amount of a pharmaceutically acceptable salt thereof, wherein the peptidomimetic macrocycle binds to MDM2 and/or MDMX proteins.
 229. The method of claim 228, wherein the peptidomimetic macrocycle disrupts the interaction between p53 and MDM2 and MDMX.
 230. The method of claim 228, further comprising confirming the lack of the p53 deactivating mutation in the solid tumor prior to the administration of the pharmaceutical composition.
 231. The method of claim 230, wherein the confirming the lack of the p53 deactivating mutation comprises confirming the presence of wild type p53 in the solid tumor.
 232. The method of claim 230, wherein the determining or the confirming is performed up to about 3 years prior to the administration of the pharmaceutical composition.
 233. The method of claim 228, wherein a dose of the pharmaceutical composition is administered one, two or three times a week.
 234. The method of claim 228, wherein a dose of the pharmaceutical composition is administered on days 1, 8 and 15 of a 28-day cycle.
 235. The method of claim 228, wherein a dose of the pharmaceutical composition is administered on days 1, 4, 8 and 11 of a 21-day cycle.
 236. The method of claim 228, wherein the amount of the peptidomimetic macrocycle or a pharmaceutically acceptable salt thereof administered is about 0.5-20 mg per kilogram body weight of the human subject.
 237. The method of claim 228, wherein the amount of the peptidomimetic macrocycle or a pharmaceutically acceptable salt thereof administered is about 0.04 mg, 0.08 mg, 0.16 mg, 0.32 mg, 0.64 mg, 1.28 mg, 3.56 mg, 7.12 mg, or 14.24 mg per kilogram body weight of the human subject.
 238. The method of claim 228, wherein the amount of the peptidomimetic macrocycle or a pharmaceutically acceptable salt thereof administered is about 0.32 mg, 0.64 mg, 1.25 mg, 2.5 mg, 5.0 mg 10.0 mg, or 20.0 mg per kilogram body weight of the human subject and the pharmaceutical composition is administered two times a week.
 239. The method of claim 228, wherein the peptidomimetic macrocycle or a pharmaceutically acceptable salt thereof administered is about 0.32 mg, 0.64 mg, 1.25 mg 2.5 or 5.0 mg per kilogram body weight of the human subject and the pharmaceutical composition is administered on day 1, 4, 8, 11 of a 21-day cycle.
 240. The method of claim 228, wherein the amount of the peptidomimetic macrocycle or a pharmaceutically acceptable salt thereof administered is about 1.25 mg, 2.5 mg, 5.0 mg 10.0 mg, or 20.0 mg per kilogram body weight of the human subject and the pharmaceutical composition is administered once a week.
 241. The method of claim 228, wherein the pharmaceutical composition is administered over a period of 0.25-2.0 h.
 242. The method of claim 228, wherein the solid tumor is selected from a group consisting of bladder cancer, bone cancer, breast cancer, cervical cancer, CNS cancer, colon cancer, ocular tumor, renal cancer, liver cancer, lung cancer, pancreatic cancer, choriocarcinoma (tumor of the placenta), prostate cancer, sarcoma, skin cancer, soft tissue cancer, gastric cancer, gall bladder cancer, biliary cancer, renal cancer, neoblastoma, a cancer that is not a HPV positive cancer or neuroendocrine cancer.
 243. The method of claim 228, wherein the pharmaceutical composition is administered intravenously.
 244. The method of claim 228, wherein the p53 deactivating mutation comprises a missense mutation or a mutation in DNA-binding domain of the protein.
 245. The method of claim 228, wherein the p53 deactivating mutation is a dominant deactivating mutation.
 246. The method of claim 228, wherein the p53 deactivating mutation comprises one or more mutations selected from a group consisting of V173L, R175H, G245C, R248W, R249S and R273H.
 247. The method of claim 228, wherein the pharmaceutical composition comprises the pharmaceutically acceptable salt of the peptidomimetic macrocycle.
 248. The method of claim 228, wherein the peptidomimetic macrocycle comprises an amino acid sequence which is at least about 60%, 70%, 80%, 90%, or 95% identical to an amino acid sequence in any of Table 3, Table 3a, Table 3b, and Table 3c, wherein the peptidomimetic macrocycle has a Formula (I):

wherein: each A, C, D and E is independently an amino acid; each B is independently an amino acid,

[—NH-L₃-CO—], [—NH-L₃-SO₂—], or [—NH-L₃-]; each R₁ and R₂ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids; each R₃ independently is hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅; each L and L′ is independently a macrocycle-forming linker of the formula -L₁-L₂-; each L₁, L₂, and L₃ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄—K—R₄—]_(n), each being optionally substituted with R₅; each R₄ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene; each K is independently O, S, SO, SO₂, CO, CO₂, or CONR₃; each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₇ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue; each R₈ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue; each v is independently an integer; each w is independently an integer from 3-1000; u is an integer from 1-10; each x, y and z is independently an integer from 0-10; and each n is independently an integer from 1-5.
 249. The method of any one of claim 248, wherein w is 1, 2, 3, 4, 5, 6, 7, 8, 9, or
 10. 250. The method of any one of claim 248, wherein v is 1-10.
 251. The method of claim 248, wherein each L₁ and L₂ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, or heterocycloarylene, each being optionally substituted with R₅.
 252. The method of any one of claim 248, wherein each R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-.
 253. The method of claim 248, wherein x+y+z=6.
 254. A method of treating solid tumor in a human subject, wherein the method comprises administering to the human subject 0.5-20 mg of a peptidomimetic macrocycle per kilogram body weight of the human subject or a pharmaceutically acceptable salt thereof on days 1, 8 and 15 of a 28-day cycle.
 255. The method of claim 254, wherein the solid tumor is determined to lack a p53 deactivating mutation.
 256. A method of treating solid tumor in a human subject, wherein the method comprises administering to the human subject 0.32-10 mg of a peptidomimetic macrocycle per kilogram body weight of the human subject or a pharmaceutically acceptable salt thereof on days 1, 4, 8 and 11 of a 21-day cycle.
 257. The method of claim 256, wherein the solid tumor is determined to lack a p53 deactivating mutation. 